Tuesday, October 25, 2016

Prevident 5000 Sensitive


Generic Name: fluoride topical (FLOR ide TOP i kal)

Brand Names: ACT Fluoride Rinse, ACT Kids Fluoride Rinse, ACT Restoring Mouthwash Cinnamon, ACT Restoring Mouthwash Mint, ACT Restoring Mouthwash Spearmint, ACT Restoring Mouthwash Vanilla Mint, Control Rx, Denta 5000 Plus, Dentagel, Ethedent, Fluoridex, Fluoridex Daily Defense, Fluoridex Daily Defense Enhanced Whitening, Fluorigard, Fluorinse, Gel-Kam, Gel-Kam Dental Therapy Pak, Gel-Kam Dentinbloc, Gel-Kam Sensitivity Therapy, NaFrinse Daily/Acidulated, NaFrinse Daily/Neutral, Nafrinse Solution, NaFrinse Weekly, Neutracare Gel, Neutragard, Neutragard Advanced, Neutral Sodium Fluoride Rinse, Omnii Gel, Omnii Gel Just For Kids, Oral B Anti-Cavity, Perfect Choice, Perio Med, Phos-Flur, Prevident, Prevident 500 Plus Boost, PreviDent 5000 Booster, Prevident 5000 Dry Mouth, Prevident 5000 Plus, Prevident 5000 Sensitive, Prevident Dental Rinse, SF, SF 5000 Plus, Stop, Thera-Flur-N


What is Prevident 5000 Sensitive (fluoride topical)?

Fluoride is a substance that strengthens tooth enamel. This helps to prevent dental cavities.


Fluoride topical is used as a medication to prevent tooth decay in patients that have a low level of fluoride topical in their drinking water. Fluoride topical is also used to prevent tooth decay in patients who undergo radiation of the head and/or neck, which may cause dryness of the mouth and an increased incidence of tooth decay.


Fluoride may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Prevident 5000 Sensitive (fluoride topical)?


Fluoride topical should not be used if the level of fluoride in the drinking water is greater than 0.7 parts per million (ppm).

Before using fluoride topical, tell your dentist and doctor if you are on a low salt or a salt free diet. You may not be able to use fluoride topical, or you may need special tests while you are using it.


Do not eat, drink, or rinse your mouth for 30 minutes after using a fluoride topical. Do not swallow fluoride topical. Spit it out after use. Do not allow a child to swallow fluoride topical or serious overdose symptoms could result.

Overdose symptoms may result if you swallow large amounts of fluoride while using it.


What should I discuss with my healthcare provider before using Prevident 5000 Sensitive (fluoride topical)?


Fluoride topical should not be used if the level of fluoride in the drinking water is greater than 0.7 parts per million (ppm).

Before using fluoride topical, tell your dentist and doctor if you are on a low salt or a salt free diet. You may not be able to use fluoride topical, or you may need special tests while you are using it.


If you have gum disease, some forms of fluoride topical may be irritating to your gums. Talk to your dentist or doctor if you have bothersome mouth irritation while using fluoride topical.


Talk to your doctor and dentist before using fluoride topical if you are pregnant. Talk to your doctor and dentist before using fluoride topical if you are breast-feeding. The use of fluoride is particularly important in children to protect against tooth decay. The American Dental Association's Council on Dental Therapeutics recommends the use of fluoride by children up to 13 years of age. The American Academy of Pediatrics recommends fluoride supplementation in children until the age of 16 years old. Do not allow a child to swallow fluoride topical or serious overdose symptoms could result.

How should I use Prevident 5000 Sensitive (fluoride topical)?


Use this medication exactly as directed on the label, or as it was prescribed by your dentist or doctor. Do not use it in larger amounts or for longer than recommended. Follow the directions on your prescription label.


Fluoride topical should be used immediately after brushing or flossing your teeth. For best results, use the medication just before bedtime, unless your doctor tells you otherwise.


Swish this medication in your mouth without swallowing. Then spit it out.


Do not eat, drink, or rinse your mouth for 30 minutes after using fluoride topical. Store fluoride topical at room temperature away from moisture and heat.

What happens if I miss a dose?


Use the missed dose as soon as you remember. If it is almost time for your next dose, wait until then to use the medicine and skip the missed dose. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include nausea, vomiting, stomach pain, diarrhea, drooling, numbness or tingling, loss of feeling anywhere in your body, muscle stiffness, or seizure (convulsions).


Overdose symptoms may result if you swallow large amounts of fluoride while using it.


What should I avoid while using Prevident 5000 Sensitive (fluoride topical)?


Do not swallow fluoride topical. Spit it out after use.

Prevident 5000 Sensitive (fluoride topical) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor if you have any of the following side effects:

  • discolored teeth;




  • weakened tooth enamel; or




  • any changes in the appearance of your teeth.



Less serious side effects may include:



  • stomach upset;




  • headache; or




  • weakness.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Prevident 5000 Sensitive (fluoride topical)?


It is not likely that other drugs you take orally or inject will have an effect on topically applied fluoride. But many drugs can interact with each other. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More Prevident 5000 Sensitive resources


  • Prevident 5000 Sensitive Side Effects (in more detail)
  • Prevident 5000 Sensitive Use in Pregnancy & Breastfeeding
  • 0 Reviews for Prevident 5000 Sensitive - Add your own review/rating


  • Prevident 5000 Sensitive Prescribing Information (FDA)

  • APF Gel Advanced Consumer (Micromedex) - Includes Dosage Information

  • EtheDent Chewable Tablets MedFacts Consumer Leaflet (Wolters Kluwer)

  • Gel-Kam Rinse MedFacts Consumer Leaflet (Wolters Kluwer)

  • Phos-Flur Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • PreviDent 5000 Sensitive MedFacts Consumer Leaflet (Wolters Kluwer)

  • Prevident 5000 Booster Prescribing Information (FDA)

  • Prevident 5000 Dry Mouth Prescribing Information (FDA)

  • Prevident 5000 Enamel Protect Prescribing Information (FDA)



Compare Prevident 5000 Sensitive with other medications


  • Prevention of Dental Caries


Where can I get more information?


  • Your pharmacist can provide more information about fluoride topical.

See also: Prevident 5000 Sensitive side effects (in more detail)


Excedrin Tension Headache


Generic Name: acetaminophen and caffeine (a SEET a MIN oh fen and KAF een)

Brand Names: Excedrin Quick Tab Peppermint, Excedrin Quick Tab Spearmint, Excedrin Tension Headache, Excedrin Tension Headache Caplet, Excedrin Tension Headache Express Gels, Excedrin Tension Headache Geltab, Valorin Extra


What is Excedrin Tension Headache (acetaminophen and caffeine)?

Acetaminophen is a pain reliever and a fever reducer.


Caffeine is used in this product to increase the pain relieving effects of acetaminophen.


The combination of acetaminophen and caffeine is used to treat pain from conditions such as headache, muscle aches, menstrual cramps, arthritis, backache, toothaches, colds and fevers.


Acetaminophen and caffeine may also be used for purposes not listed in this medication guide.


What is the most important information I should know about Excedrin Tension Headache (acetaminophen and caffeine)?


Do not take this medication without a doctor's advice if you have ever had alcoholic liver disease (cirrhosis) or if you drink more than 3 alcoholic beverages per day. You may not be able to take medicine that contains acetaminophen. Do not take more of this medication than is recommended. An overdose of acetaminophen can damage your liver or cause death. Ask a doctor or pharmacist before using any other cold, allergy, pain, or sleep medication. Acetaminophen (sometimes abbreviated as APAP) is contained in many combination medicines. Taking certain products together can cause you to get too much acetaminophen which can lead to a fatal overdose. Check the label to see if a medicine contains acetaminophen or APAP. Avoid drinking alcohol. It may increase your risk of liver damage while taking acetaminophen.

What should I discuss with my healthcare provider before taking Excedrin Tension Headache (acetaminophen and caffeine)?


Do not take this medication if you are allergic to acetaminophen (Tylenol) or caffeine. Do not take this medication without a doctor's advice if you have ever had alcoholic liver disease (cirrhosis) or if you drink more than 3 alcoholic beverages per day. You may not be able to take medicine that contains acetaminophen.

Ask a doctor or pharmacist if it is safe for you to take this medicine if you have kidney or liver disease, or a history of alcoholism.


It is not known whether this medicine will harm an unborn baby. Do not take acetaminophen and caffeine without medical advice if you are pregnant. Acetaminophen and caffeine can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I take Excedrin Tension Headache (acetaminophen and caffeine)?


Use this medication exactly as directed on the label, or as prescribed by your doctor.


Do not take more of this medication than is recommended. An overdose of acetaminophen can damage your liver or cause death.

One acetaminophen and caffeine pill contains 500 mg of acetaminophen. Know the amount of acetaminophen in the specific product you are taking.


The orally disintegrating tablet (Excedrin QuickTabs) should be placed directly on the tongue. Do not swallow the tablet whole. Allow it to dissolve in your mouth without chewing. Swallow several times as the tablet dissolves. If desired, you may drink liquid to help swallow the dissolved tablet.


Call your doctor if your symptoms do not improve, especially if you still have a fever after 3 days of using this medication, or pain after 10 days of use. Stop taking acetaminophen and caffeine and call your doctor at any time if your symptoms get worse.

Acetaminophen may cause false urine glucose test results. Talk to your doctor if you have diabetes and you notice changes in glucose test results while taking acetaminophen and caffeine.


Store at room temperature away from heat and moisture.

What happens if I miss a dose?


Since acetaminophen and caffeine is taken as needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include loss of appetite, confusion, nausea, vomiting, diarrhea, sweating, fast or uneven heart rate, seizure (convulsions), pain in your upper stomach, dark urine, and yellowing of your skin or the whites of your eyes.


What should I avoid while taking Excedrin Tension Headache (acetaminophen and caffeine)?


Ask a doctor or pharmacist before using any other cold, allergy, pain, or sleep medication. Acetaminophen (sometimes abbreviated as APAP) is contained in many combination medicines. Taking certain products together can cause you to get too much acetaminophen which can lead to a fatal overdose. Check the label to see if a medicine contains acetaminophen or APAP. Avoid drinking alcohol. It may increase your risk of liver damage while taking acetaminophen. Avoid coffee, tea, cola, energy drinks or other sources of caffeine while taking this medication. They can add to the side effects of the caffeine in the medication.

Excedrin Tension Headache (acetaminophen and caffeine) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using acetaminophen and caffeine and call your doctor at once if you have a serious side effect such as:

  • low fever with nausea, stomach pain, and loss of appetite;




  • dark urine, clay-colored stools; or




  • jaundice (yellowing of the skin or eyes).



Less serious side effects may include:



  • sleep problems (insomnia); or




  • feeling nervous, irritable, or jittery.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Excedrin Tension Headache (acetaminophen and caffeine)?


There may be other drugs that can interact with acetaminophen and caffeine. Tell your doctor about all medications you use. This includes prescription, over the counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Excedrin Tension Headache resources


  • Excedrin Tension Headache Side Effects (in more detail)
  • Excedrin Tension Headache Use in Pregnancy & Breastfeeding
  • Excedrin Tension Headache Drug Interactions
  • Excedrin Tension Headache Support Group
  • 2 Reviews for Excedrin Tension Headache - Add your own review/rating


Compare Excedrin Tension Headache with other medications


  • Cold Symptoms
  • Headache
  • Osteoarthritis
  • Pain
  • Period Pain
  • Sinusitis


Where can I get more information?


  • Your pharmacist can provide more information about acetaminophen and caffeine.

See also: Excedrin Tension Headache side effects (in more detail)


Fluvastatin-Teva




Fluvastatin-Teva may be available in the countries listed below.


Ingredient matches for Fluvastatin-Teva



Fluvastatin

Fluvastatin sodium salt (a derivative of Fluvastatin) is reported as an ingredient of Fluvastatin-Teva in the following countries:


  • Germany

  • Slovakia

  • Switzerland

International Drug Name Search

paclitaxel protein-bound


Generic Name: paclitaxel protein-bound (PAK li TAX el PRO teen-bound)

Brand Names: Abraxane


What is paclitaxel protein-bound?

Paclitaxel protein-bound is a cancer medication that interferes with the growth and spread of cancer cells in the body.


Paclitaxel protein-bound is used in the treatment of breast cancer.


Paclitaxel protein-bound is usually given after other cancer medicines have been tried without successful treatment.


Paclitaxel protein-bound may also be used for purposes not listed in this medication guide.


What is the most important information I should know about paclitaxel protein-bound?


Do not use paclitaxel protein-bound if you are pregnant. It could harm the unborn baby. Use birth control to prevent pregnancy while you are receiving paclitaxel protein-bound, whether you are a man or a woman. Paclitaxel protein-bound use by either parent may cause birth defects. You should not use paclitaxel protein-bound if you are allergic to it, or if you have a low white blood cell count.

Before you receive this medication, tell your doctor if you have kidney disease, liver disease, heart disease, or bone marrow suppression.


To make sure this medication is helping your condition and not causing harmful effects, your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests. Do not miss any follow-up visits to your doctor.


Call your doctor at once if you have a serious side effect such as fever, chills, flu symptoms, mouth sores, easy bruising or bleeding, pale skin, feeling light-headed or short of breath, swelling or rapid weight gain, chest pain, sudden cough, rapid heart rate, or trouble breathing.

What should I discuss with my healthcare provider before receiving paclitaxel protein-bound?


You should not use paclitaxel protein-bound if you are allergic to it, or if you have a low white blood cell count.

To make sure you can safely receive paclitaxel protein-bound, tell your doctor if you have any of these other conditions:



  • kidney disease;




  • liver disease;




  • heart disease; or




  • bone marrow suppression.




FDA pregnancy category D. Do not use paclitaxel protein-bound if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment. Use birth control to prevent pregnancy while you are receiving paclitaxel protein-bound, whether you are a man or a woman. Paclitaxel protein-bound use by either parent may cause birth defects. It is not known whether paclitaxel protein-bound passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are receiving paclitaxel protein-bound.

How is paclitaxel protein-bound given?


Paclitaxel protein-bound is injected into a vein through an IV. You will receive this injection in a clinic or hospital setting. Paclitaxel protein-bound must be given slowly, and the IV infusion can take at least 30 minutes to complete.


Paclitaxel protein-bound is usually given once every 3 weeks. Follow your doctor's dosing instructions very carefully.


Tell your caregivers if you feel any burning, pain, or swelling around the IV needle when paclitaxel protein-bound is injected.

To make sure this medication is helping your condition and not causing harmful effects, your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests. Do not miss any follow-up visits to your doctor.


What happens if I miss a dose?


Call your doctor for instructions if you miss an appointment for your paclitaxel protein-bound injection.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include some of the serious side effects listed in this medication guide.


What should I avoid while using paclitaxel protein-bound?


Paclitaxel protein-bound can be harmful if it gets in your eyes, mouth, or nose, or on your skin. If skin contact occurs, wash the area with soap and water or rinse the eyes thoroughly with plain water.

Paclitaxel protein-bound side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

  • fever, chills, body aches, flu symptoms, sores in your mouth and throat;




  • easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin;




  • pale skin, feeling light-headed or short of breath, rapid heart rate, trouble concentrating;




  • feeling like you might pass out;




  • swelling, rapid weight gain; or




  • chest pain, sudden cough, wheezing, trouble breathing, fast heart rate.



Less serious side effects may include:



  • numbness or tingly feeling;




  • muscle or joint pain;




  • nausea, vomiting;




  • diarrhea; or




  • hair loss.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


Paclitaxel protein-bound Dosing Information


Usual Adult Dose for Breast Cancer:

260 mg/m2 administered intravenously over 30 minutes every 3 weeks


What other drugs will affect paclitaxel protein-bound?


Tell your doctor about all other medicines you use, especially:



  • bosentan (Tracleer);




  • conivaptan (Vaprisol);




  • imatinib (Gleevec);




  • isoniazid (for treating tuberculosis);




  • montelukast (Singulair) or zafirlukast (Accolate);




  • rifampin (Rifater, Rifadin, Rifamate);




  • selegiline (Eldepryl, Emsam, Zelapar);




  • an antibiotic such as clarithromycin (Biaxin), dalfopristin/quinupristin (Synercid), erythromycin (E.E.S., EryPed, Ery-Tab, Erythrocin), or telithromycin (Ketek);




  • an antidepressant such as nefazodone or fluoxetine (Prozac);




  • antifungal medication such as clotrimazole (Mycelex Troche), itraconazole (Sporanox), ketoconazole (Extina, Ketozole, Nizoral, Xolegal), or voriconazole (Vfend);




  • a blood thinner such as warfarin (Coumadin);




  • cancer medication such as paclitaxel (Taxol) or tamoxifen (Soltamox);




  • heart or blood pressure medications such as amiodarone (Cordarone, Pacerone), carvedilol (Coreg), diltiazem (Cartia, Cardizem), felodipine (Plendil), losartan (Hyzaar, Cozaar), nifedipine (Nifedical, Procardia), torsemide (Demadex), verapamil (Calan, Covera, Isoptin, Verelan), and others;




  • HIV/AIDS medicine such as atazanavir (Reyataz), delavirdine (Rescriptor), fosamprenavir (Lexiva), indinavir (Crixivan), nelfinavir (Viracept), saquinavir (Invirase), or ritonavir (Norvir);




  • seizure medications such as fosphenytoin (Cerebyx), or phenytoin (Dilantin);




  • oral diabetes medication such as glimepiride (Amaryl), glipizide (Glucotrol), nateglinide (Starlix), pioglitazone (Actos, Actoplus Met), repaglinide (Prandin), rosiglitazone (Avandia, Avandamet), or tolbutamide (Orinase); or




  • sulfa drugs (Bactrim, Gantanol, Gantrisin, Septra, SMX-TMP, and others).



This list is not complete and other drugs may interact with paclitaxel protein-bound. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More paclitaxel protein-bound resources


  • Paclitaxel protein-bound Side Effects (in more detail)
  • Paclitaxel protein-bound Dosage
  • Paclitaxel protein-bound Use in Pregnancy & Breastfeeding
  • Paclitaxel protein-bound Drug Interactions
  • Paclitaxel protein-bound Support Group
  • 1 Review for Paclitaxel protein-bound - Add your own review/rating


  • paclitaxel protein-bound Intravenous Advanced Consumer (Micromedex) - Includes Dosage Information

  • Abraxane Prescribing Information (FDA)

  • Abraxane MedFacts Consumer Leaflet (Wolters Kluwer)

  • Abraxane Consumer Overview



Compare paclitaxel protein-bound with other medications


  • Breast Cancer
  • Breast Cancer, Metastatic


Where can I get more information?


  • Your doctor or pharmacist can provide more information about paclitaxel protein-bound.

See also: paclitaxel protein-bound side effects (in more detail)


Monday, October 24, 2016

Ertaczo


Generic Name: sertaconazole topical (ser ta CAW nah zole)

Brand Names: Ertaczo


What is sertaconazole topical?

Sertaconazole topical is an antifungal medication. Sertaconazole topical prevents fungus from growing on the skin.


Sertaconazole topical is used to treat fungal infections of the skin such as athlete's foot.


Sertaconazole topical may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about sertaconazole topical?


Use this medication for the full amount of time prescribed. Your symptoms may start to improve before the infection is completely healed, however it is important to complete the full course of treatment.

Do not use bandages or dressings that do not allow air circulation over the affected area (occlusive dressings) unless otherwise directed by your doctor. If the affected area is the feet, be sure to wear clean, cotton socks and sandals or shoes that allow air circulation.


Do not get this medication in the eyes, nose, or mouth. If this happens, rinse with water and seek medical attention if irritation occurs.

What should I discuss with my healthcare provider before using sertaconazole topical?


Do not use sertaconazole topical without first talking to your doctor if you have had an allergic reaction to it in the past.


Sertaconazole topical is in the FDA pregnancy category C. This means that it is not known whether sertaconazole topical will be harmful to an unborn baby. Do not use this medication without first talking to your doctor if you are pregnant or could become pregnant during treatment. It is not known whether sertaconazole passes into breast milk. Do not use sertaconazole topical without first talking to your doctor if you are breast-feeding a baby.

How should I use sertaconazole topical?


Use sertaconazole exactly as directed by your doctor. If you do not understand these instructions, ask your pharmacist, nurse, or doctor to explain them to you.

Wash your hands before and after using this medication.


If the cream is used after bathing or showering, dry the skin thoroughly before application.


Apply the cream to the affected area twice a day as directed by your healthcare provider.


Use this medication for the full amount of time prescribed. Your symptoms may start to improve before the infection is completely healed, however it is important to complete the full course of treatment.

It is important to use sertaconazole topical regularly to get the most benefit.


If the infection does not clear up in a few weeks, or if it appears to get worse, contact your doctor.


Do not use bandages or dressings that do not allow air circulation over the affected area (occlusive dressings) unless otherwise directed by your doctor. If the affected area is the feet, be sure to wear clean, cotton socks and sandals or shoes that allow air circulation.


Do not get this medication in the eyes, nose, or mouth. If this happens, rinse with water and seek medical attention if irritation occurs. Store sertaconazole topical at room temperature away from moisture and heat.

What happens if I miss a dose?


Apply the missed dose as soon as you remember. However, if it is almost time for the next regularly scheduled dose, skip the dose you missed and apply only the regular amount of sertaconazole topical. Do not use a double dose unless otherwise directed by your doctor.


What happens if I overdose?


An overdose of sertaconazole topical is unlikely to threaten life. If an overdose is suspected or if sertaconazole topical has been ingested, contact an emergency room or a poison control center for advice.


What should I avoid while using sertaconazole topical?


Do not use bandages or dressings that do not allow air circulation over the affected area (occlusive dressings) unless otherwise directed by your doctor. A light cotton-gauze dressing may be used to protect clothing, unless otherwise directed by your doctor. If the affected area is the feet, be sure to wear clean, cotton socks and sandals or shoes that allow air circulation.


Sertaconazole topical side effects


Serious side effects are not expected to occur with the use of sertaconazole topical. Stop using sertaconazole topical and contact your doctor if you experience unusual or severe itching, redness, burning, blistering, swelling, oozing, or irritation of the skin.


Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect sertaconazole topical?


Do not use other topical products on the treated area, unless otherwise directed by your doctor. Other topical products may affect the absorption or effectiveness of sertaconazole topical.

Although it is unlikely that sertaconazole topical will interact with other medications taken by mouth, some interactions may occur. Talk to your doctor and pharmacist before taking or using any prescription or over-the-counter medicines, including vitamins, minerals, and herbal products.



More Ertaczo resources


  • Ertaczo Side Effects (in more detail)
  • Ertaczo Use in Pregnancy & Breastfeeding
  • Ertaczo Support Group
  • 0 Reviews for Ertaczo - Add your own review/rating


  • Ertaczo Prescribing Information (FDA)

  • Ertaczo Monograph (AHFS DI)

  • Ertaczo Topical Advanced Consumer (Micromedex) - Includes Dosage Information

  • Ertaczo MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ertaczo Consumer Overview



Compare Ertaczo with other medications


  • Tinea Pedis


Where can I get more information?


  • Your pharmacist has additional information about sertaconazole written for health professionals that you may read.

See also: Ertaczo side effects (in more detail)


Friday, October 21, 2016

gentamicin



Generic Name: gentamicin (gen tah MY sin)

Brand names: Garamycin, Cidomycin, Septopal


What is gentamicin?

Gentamicin is an antibiotic. It fights bacteria in the body.


Gentamicin is used to treat severe or serious bacterial infections.


Gentamicin may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about gentamicin?


If you are injecting gentamicin at home, your healthcare provider will give you detailed instructions on how and where to inject the medication. If you do not understand these directions, do not attempt to inject the medication. Contact your healthcare provider for further instructions.


Gentamicin may cause damage to the kidneys and/or nerves. Kidney function and drug levels in the blood may be monitored with blood tests during treatment. Tell your doctor if you experience hearing loss, dizziness, numbness, skin tingling, muscle twitching, or seizures which may be signs of nerve damage.


What should I discuss with my healthcare provider before using gentamicin?


Do not use gentamicin without first talking to your doctor if you have

  • sulfite sensitivity;



  • kidney disease;


  • hearing loss or loss of balance due to ear problems;




  • Parkinson's disease; or




  • a neuromuscular disorder such as myasthenia gravis.



You may not be able to use gentamicin, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above.


Do not use gentamicin without first talking to your doctor if you are pregnant or could become pregnant during treatment. Do not use gentamicin without first talking to your doctor if you are breast-feeding a baby.

How should I take gentamicin?


If you are injecting gentamicin at home, your healthcare provider will give you detailed instructions on how and where to inject the medication. If you do not understand these directions, do not attempt to inject the medication. Contact your healthcare provider for further instructions.


Do not use any gentamicin that is discolored, has particles in it, or looks different from your previous doses. Throw away any unused gentamicin after the amount of time determined by your pharmacist or doctor.


Adequate hydration is important during treatment with gentamicin. Fluids may be administered intravenously during treatment.


It is important that the medication be given on a regular schedule and for the entire amount of time prescribed by your doctor.


Gentamicin may cause damage to the kidneys and/or nerves. Kidney function and drug levels in the blood may be monitored with blood tests during treatment. Tell your doctor if you experience hearing loss, dizziness, numbness, skin tingling, muscle twitching, or seizures which may be signs of nerve damage.


Dispose of used needles and syringes in a puncture resistant container out of the reach of children.


Your healthcare provider will store gentamicin as directed by the manufacturer or give you detailed storage instructions if you are storing the medication at home.


See also: Gentamicin dosage (in more detail)

What happens if I miss a dose?


Contact your doctor if a dose is missed.


What happens if I overdose?


Contact your doctor or seek emergency medical attention if an overdose is suspected. An overdose of the medication may result in damage to the kidneys or hearing loss, dizziness, numbness, skin tingling, muscle twitching, or seizures (which may be signs of nerve damage).


What should I avoid while taking gentamicin?


There are no restrictions on food, beverages, or activity while taking gentamicin unless otherwise directed by your doctor.


Gentamicin side effects


If you experience any of the following serious side effects, stop taking gentamicin and seek emergency medical attention:

  • an allergic reaction (shortness of breath; closing of the throat; hives; swelling of the lips, face, or tongue; rash; or fainting);




  • little or no urine;




  • decreased hearing or ringing in the ears;




  • dizziness, clumsiness, or unsteadiness;




  • numbness, skin tingling, muscle twitching, or seizures; or




  • severe watery diarrhea and abdominal cramps.



Other, less serious side effects may be more likely to occur. Continue to take gentamicin and talk to your doctor if you experience



  • increased thirst;




  • loss of appetite;




  • nausea or vomiting;




  • a rash.



Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. You may report side effects to FDA at 1-800-FDA-1088.


Gentamicin Dosing Information


Usual Adult Dose for Bacteremia:

1.5 to 2 mg/kg loading dose, followed by 1 to 1.7 mg/kg IV or IM every 8 hours or 5 to 7 mg/kg IV every 24 hours.
Duration: 14 days, depending on the site, nature and severity of the bacteremia. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient is stable for at least 48 hours, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Adult Dose for Bacterial Endocarditis Prophylaxis:

1.5 mg/kg (maximum 120 mg) IV or IM once within 30 minutes of starting the procedure. For high risk patients, in addition to gentamicin, ampicillin 2 g is given IV or IM 30 minutes prior to the procedure, followed by ampicillin 1 g IV/IM or amoxicillin 1 g orally 6 hours later. In penicillin-allergic patients, vancomycin 1 g is infused intravenously 1 to 2 hours prior to the procedure.

Usual Adult Dose for Bacterial Infection:

1.5 to 2 mg/kg loading dose, followed by 1 to 1.7 mg/kg IV or IM every 8 hours, or 5 to 7 mg/kg IV every 24 hours.
Duration: 7 to 21 days, depending on the nature and severity of the infection. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient is stable for at least 48 hours, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Adult Dose for Brucellosis:

2 mg/kg loading dose, followed by 1.7 mg/kg IV or IM every 8 hours or 5 mg/kg IV every 24 hours.
Duration: Gentamicin should be continued for the first 2 to 3 weeks of antibiotic therapy. Oral doxycycline or sulfamethoxazole/trimethoprim should be continued for at least 6 weeks.

Usual Adult Dose for Burns - External:

2 to 2.5 mg/kg loading dose, followed by 1.7 to 2 mg/kg IV every 8 hours
Duration: 10 to 14 days, depending on the nature and severity of the infection

Usual Adult Dose for Cystic Fibrosis:

5 to 10 mg/kg/day in 2 to 4 divided doses
Duration: Parenteral therapy should be continued for about 14 to 21 days, depending on the nature and severity of the infection and improvement of pulmonary function.

Usual Adult Dose for Endocarditis:

Native valve infections due to highly penicillin-susceptible viridans Group streptococci and S bovis (MIC Duration: 2 weeks; continue other antibiotic for 4 weeks

Native valve infections due to relatively penicillin-resistant S viridans and S bovis (MIC > 0.12 mcg/mL and Duration: 2 weeks; continue other antibiotic for 4 weeks

Prosthetic valve infections due to S viridans and S bovis:
3 mg/kg IV or IM once every 24 hours in combination with aqueous penicillin G or ceftriaxone.
Duration: 2 weeks; continue other antibiotic for 6 weeks

Native valve infections due to staphylococci:
1.5 mg/kg IV or IM every 12 hours or 1 mg/kg every 8 hours, in combination with nafcillin, oxacillin, or cefazolin
Duration: 3 to 5 days; continue other antibiotic for 6 weeks

Prosthetic valve infections due to staphylococci:
1.5 mg/kg IV or IM every 12 hours or 1 mg/kg every 8 hours, in combination with nafcillin or oxacillin, plus rifampin, or vancomycin plus rifampin.
Duration: 2 weeks; continue other antibiotics for 6 weeks

Native valve or prosthetic valve infections due to susceptible enterococci:
1 mg/kg IV or IM every 8 hours, in combination with ampicillin, aqueous penicillin G, or vancomycin.
Duration: 4 to 6 weeks; continue other antibiotic for 6 weeks

Native valve or prosthetic valve infections due to penicillin-resistant enterococci:
1 mg/kg IV or IM every 8 hours, in combination with ampicillin-sulbactam or vancomycin.
Duration: 6 weeks

Refer to current published guidelines for detailed recommendations.

Usual Adult Dose for Endometritis:

2 mg/kg loading dose, followed by 1.5 mg/kg IV or IM every 8 hours.
Duration: Parenteral therapy should be continued for at least 24 hours after the patient has remained afebrile, pain free, and the leukocyte count has normalized.

Usual Adult Dose for Febrile Neutropenia:

2 mg/kg loading dose, followed by 1.7 mg/kg IV every 8 hours.
Duration: Once the patient is stable, afebrile for 24 hours, and the absolute neutrophil count is greater than 500/mm3, oral antibiotics may be substituted if antibiotic therapy is to be continued.

Usual Adult Dose for Intraabdominal Infection:

2 mg/kg loading dose, followed by 1.7 mg/kg IV every 8 hours or 5 mg/kg IV every 24 hours
Duration: 14 days, depending on the nature and severity of the infection. Less toxic antibiotics may be substituted once the patient is stable for at least 48 hours.

Usual Adult Dose for Meningitis:

Intravenous/Intramuscular: 2 mg/kg loading dose, followed by 1.7 mg/kg every 8 hours. Duration: Parenteral therapy should be continued for at least one week after the patient becomes afebrile and cerebrospinal fluid normalizes.

Usual Adult Dose for Osteomyelitis:

1.5 to 2 mg/kg loading dose, followed by 1 to 1.7 mg/kg IV or IM every 8 hours or 5 to 7 mg/kg IV every 24 hours.
Duration: 4 to 6 weeks, depending on the nature and severity of the infection. Chronic osteomyelitis may require an additional 1 to 2 months of oral antibiotics. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient is stable for at least 48 hours, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Adult Dose for Pelvic Inflammatory Disease:

2 mg/kg loading dose, followed by 1.5 mg/kg IV or IM every 8 hours or 5 mg/kg IV every 24 hours.
Duration: Parenteral therapy should be continued for at least 24 hours after clinical improvement and should followed by oral doxycycline or clindamycin for a total 14 day course.

Usual Adult Dose for Peritonitis:

IV: 2 mg/kg loading dose, followed by 1.7 mg/kg IV every 8 hours or 5 mg/kg IV every 24 hours.
Duration: Therapy should be continued for about 14 days, depending on the nature and severity of the infection. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient is stable for at least 48 hours, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Intraperitoneally in CAPD patients: 0.6 to 0.75 mg/kg intraperitoneally once daily or 16 to 20 mg per every 2 L dialysate.

Usual Adult Dose for Plague:

2 mg/kg loading dose, followed by 1.7 mg/kg IV or IM every 8 hours or 5 mg/kg IV every 24 hours.
Duration: Therapy should be continued for about 10 to 14 days, depending on the nature and severity of the infection. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient's condition improves, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Adult Dose for Pneumonia:

2 mg/kg loading dose, followed by 1.7 mg/kg IV or IM every 8 hours or 5 mg/kg IV every 24 hours.
Duration: Therapy should be continued for 14 to 21 days, depending on the nature and severity of the infection. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient is stable for at least 48 hours, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Adult Dose for Pyelonephritis:

2 mg/kg loading dose, followed by 1.7 mg/kg IV every 8 hours or 5 mg/kg IV every 24 hours.
Duration: Therapy should be continued for about 7 to 14 days, depending on the nature and severity of the infection. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient is stable for at least 48 hours, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Adult Dose for Skin or Soft Tissue Infection:

1.5 to 2 mg/kg loading dose, followed by 1 to 1.7 mg/kg IV or IM every 8 hours or 5 to 7 mg/kg IV every 24 hours.
Duration: Therapy should be continued for at least 10 to 14 days, or until 3 days post acute inflammation, depending on the nature and severity of the infection. For severe infections, such as diabetic soft tissue infections, 14 to 21 days of therapy may be required. Limiting the duration of gentamicin therapy may help limit toxicity. Once the patient is stable for at least 48 hours, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Adult Dose for Surgical Prophylaxis:

1.5 to 2 mg/kg (maximum 120 mg) IV or IM once at induction of anesthesia

Usual Adult Dose for Tularemia:

1.5 to 2 mg/kg loading dose, followed by 1 to 1.7 mg/kg IV or IM every 8 hours or 5 to 7 mg/kg IV every 24 hours.
Duration: Therapy should be continued for about 10 to 14 days, depending on the nature and severity of the infection. Once the patient's condition improves, less toxic intravenous or oral antibiotic therapy may be considered according to microbiology sensitivity data.

Usual Pediatric Dose for Bacterial Infection:

0 to 4 weeks, birthweight
0 to 1 week, birthweight >=1200 g: 2.5 mg/kg IV or IM every 12 hours

1 to 4 weeks, birthweight 1200 to 2000 g: 2.5 mg/kg IV or IM every 8 to 12 hours

1 to 4 weeks, birthweight >=2000 g: 2.5 mg/kg IV or IM every 8 hours

>1 month: 1 to 2.5 mg/kg IV or IM every 8 hours

Usual Pediatric Dose for Bacterial Endocarditis Prophylaxis:

1.5 mg/kg IV or IM once within 30 minutes of starting the procedure. For high risk patients, in addition to gentamicin, ampicillin 50 mg/kg (maximum 2 G) is given IV or IM 30 minutes prior to the procedure, followed by ampicillin 25 mg/kg IV/IM or amoxicillin 25 mg/kg orally 6 hours later. In penicillin-allergic patients, vancomycin 20 mg/kg IV is infused over 1 to 2 hours instead of ampicillin/amoxicillin.

Usual Pediatric Dose for Endocarditis:

Native valve infections due to highly penicillin-susceptible viridans Group streptococci and S bovis (MIC Duration: 2 weeks; continue other antibiotic for 4 weeks

Native valve infections due to relatively penicillin-resistant S viridans and S bovis (MIC > 0.12 mcg/mL and Duration: 2 weeks; continue other antibiotic for 4 weeks

Prosthetic valve infections due to S viridans and S bovis:
3 mg/kg IV or IM once every 24 hours or 1 mg/kg every 8 hours in combination with aqueous penicillin G or ceftriaxone.
Duration: 2 weeks; continue other antibiotic for 6 weeks

Native valve infections due to staphylococci:
1 mg/kg every 8 hours, in combination with nafcillin, oxacillin, or cefazolin
Duration: 3 to 5 days; continue other antibiotic for 6 weeks

Prosthetic valve infections due to staphylococci:
1 mg/kg every 8 hours, in combination with nafcillin or oxacillin, plus rifampin, or vancomycin plus rifampin.
Duration: 2 weeks; continue other antibiotics for 6 weeks

Native valve or prosthetic valve infections due to susceptible enterococci:
1 mg/kg IV or IM every 8 hours, in combination with ampicillin, aqueous penicillin G, or vancomycin.
Duration: 4 to 6 weeks; continue other antibiotic for 6 weeks

Native valve or prosthetic valve infections due to penicillin-resistant enterococci:
1 mg/kg IV or IM every 8 hours, in combination with ampicillin-sulbactam or vancomycin.
Duration: 6 weeks

Refer to current published guidelines for detailed recommendations.

Usual Pediatric Dose for Surgical Prophylaxis:

2 mg/kg IV once at induction of anesthesia


What other drugs will affect gentamicin?


Other drugs, especially those that affect the kidneys, can interact with gentamicin resulting in dangerous side effects and/or decreased effectiveness. Do not take any other prescription or over-the-counter medicines, including vitamins, minerals, and herbal products, without first talking to your doctor during treatment with gentamicin.



More gentamicin resources


  • Gentamicin Dosage
  • Gentamicin Use in Pregnancy & Breastfeeding
  • Gentamicin Drug Interactions
  • Gentamicin Support Group
  • 0 Reviews for Gentamicin - Add your own review/rating


  • gentamicin Injection Advanced Consumer (Micromedex) - Includes Dosage Information

  • Gentamicin Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Gentamicin Professional Patient Advice (Wolters Kluwer)

  • Garamycin Solution MedFacts Consumer Leaflet (Wolters Kluwer)

  • Gentamicin Sulfate Monograph (AHFS DI)



Compare gentamicin with other medications


  • Bacteremia
  • Bacterial Endocarditis Prevention
  • Bacterial Infection
  • Bone infection
  • Brucellosis
  • Burns, External
  • Cystic Fibrosis
  • Endocarditis
  • Endometritis
  • Febrile Neutropenia
  • Intraabdominal Infection
  • Kidney Infections
  • Meningitis
  • Pelvic Inflammatory Disease
  • Peritonitis
  • Plague
  • Pneumonia
  • Rabbit Fever
  • Skin Infection
  • Surgical Prophylaxis


Where can I get more information?


  • Your pharmacist has additional information about gentamicin written for health professionals that you may read.


Méclocycline




Méclocycline may be available in the countries listed below.


Ingredient matches for Méclocycline



Meclocycline

Méclocycline (DCF) is also known as Meclocycline (Rec.INN)

International Drug Name Search

Glossary

DCFDénomination Commune Française
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Prochlorperazine Syrup



Generic Name: Prochlorperazine (pro-klor-PURR-uh-zeen)
Brand Name: Compazine


Prochlorperazine Syrup is used for:

Controlling severe nausea and vomiting and treating schizophrenia. It is also used for the short-term (4 weeks) treatment of generalized nonpsychotic anxiety. It may also be used for other conditions as determined by your doctor.


Prochlorperazine Syrup is a phenothiazine. It works by blocking a certain chemical (dopamine) in the brain.


Do NOT use Prochlorperazine Syrup if:


  • you are allergic to any ingredient in Prochlorperazine Syrup or similar medicines

  • you are taking astemizole, cisapride, or terfenadine

  • you have severe central nervous system depression

Contact your doctor or health care provider right away if any of these apply to you.



Video: Treatment for Depression







Treatments for depression are getting better everyday and there are things you can start doing right away.






Before using Prochlorperazine Syrup:


Some medical conditions may interact with Prochlorperazine Syrup. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have a history of heart disease, central nervous system depression, blood problems, liver problems, low blood pressure, increased pressure in the eye, neuroleptic malignant syndrome, tardive dyskinesia, bone marrow problems, unusual muscle movements, Parkinson disease, a predisposition to glaucoma, Reye syndrome, prostate problems, or seizures, or you have alcoholism

Some MEDICINES MAY INTERACT with Prochlorperazine Syrup. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Anticholinergics (eg, diphenhydramine, oxybutynin, scopolamine) or lithium because they may decrease Prochlorperazine Syrup's effectiveness

  • Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril), anticholinergics (eg, diphenhydramine, oxybutynin, scopolamine), general anesthetics (eg, thiopental), haloperidol, methyldopa, or tricyclic antidepressants (eg, amitriptyline) because the risk of side effects, such as seizures, may be increased

  • ACE inhibitors (eg, enalapril), anticholinergics (eg, diphenhydramine, oxybutynin, scopolamine), astemizole, cisapride, dofetilide, haloperidol, hydantoins (eg, phenytoin), methyldopa, metrizamide, naltrexone, polypeptide antibiotics (eg, actinomycin), serotonin receptor antagonist antiemetics (eg, ondansetron), terfenadine, tramadol, trazodone, or tricyclic antidepressants (eg, amitriptyline) because the risk of their side effects may be increased by Prochlorperazine Syrup

  • Bromocriptine, guanethidine, levodopa, or pergolide because their effectiveness may be decreased by Prochlorperazine Syrup

  • Lithium because unexpected toxic effects may occur

This may not be a complete list of all interactions that may occur. Ask your health care provider if Prochlorperazine Syrup may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Prochlorperazine Syrup:


Use Prochlorperazine Syrup as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Prochlorperazine Syrup by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose.

  • If you miss a dose of Prochlorperazine Syrup, take it as soon as possible. If you are taking 1 dose at bedtime and do not remember until the next morning, skip the missed dose and go back to your regular dosing schedule.

Ask your health care provider any questions you may have about how to use Prochlorperazine Syrup.



Important safety information:


  • Prochlorperazine Syrup may cause drowsiness, dizziness, blurred vision, or lightheadedness. These effects may be worse if you take it with alcohol or certain medicines. Use Prochlorperazine Syrup with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Prochlorperazine Syrup may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

  • Do not drink alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Prochlorperazine Syrup; it may add to their effects. Ask your pharmacist if you have questions about which medicines may cause drowsiness.

  • Tell your doctor or dentist that you take Prochlorperazine Syrup before you receive any medical or dental care, emergency care, or surgery.

  • Prochlorperazine Syrup may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Prochlorperazine Syrup. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

  • Avoid exposure to extreme heat while taking Prochlorperazine Syrup.

  • Patients who will be having spinal cord surgery should stop using Prochlorperazine Syrup at least 48 hours before surgery. Do not use Prochlorperazine Syrup for at least 24 hours after surgery and do not use it to control nausea and vomiting that has occurred before or after surgery.

  • Neuroleptic malignant syndrome (NMS) is a possibly fatal syndrome that can be caused by Prochlorperazine Syrup. Symptoms may include fever; stiff muscles; confusion; abnormal thinking; fast or irregular heartbeat; and sweating. Contact your doctor at once if you have any of these symptoms.

  • Use Prochlorperazine Syrup with caution in the ELDERLY; they may be more sensitive to its effects.

  • Prochlorperazine Syrup should not be used in CHILDREN who are having surgery, who are younger than 2 years old, or who weigh less than 20 pounds; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Prochlorperazine Syrup while you are pregnant. Prochlorperazine Syrup is found in breast milk. If you are or will be breast-feeding while you use Prochlorperazine Syrup, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Prochlorperazine Syrup:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Blurred vision; chills; constipation; dizziness; drowsiness; dry mouth; jitteriness; nasal congestion; sleeplessness.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); agitation; altered mental abilities, including lack of response to your surroundings; changes in breasts; changes in menstrual period; changes in vision; difficulty swallowing; drooling; excessive sweating; fever; inability to move eyes; increased body heat; involuntary movements of tongue, face, mouth, or jaw (eg, protrusion of tongue, puffing of cheeks, puckering of mouth, chewing movements); irregular or fast heartbeat; mask-like face; muscle stiffness; muscle spasms of face, neck, or back; prolonged or painful erection; restlessness; rigid muscles; shuffling walk; sore throat; tension in legs; tremors; twitching or twisting movements; unusual eye movements; weakness of arms or legs; yellowing of the skin or eyes.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Prochlorperazine side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include deep sleep or loss of consciousness; muscle spasms; restlessness; seizures; tremors; twitching.


Proper storage of Prochlorperazine Syrup:

Store Prochlorperazine Syrup at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Prochlorperazine Syrup out of the reach of children and away from pets.


General information:


  • If you have any questions about Prochlorperazine Syrup, please talk with your doctor, pharmacist, or other health care provider.

  • Prochlorperazine Syrup is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Prochlorperazine Syrup. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Prochlorperazine resources


  • Prochlorperazine Side Effects (in more detail)
  • Prochlorperazine Use in Pregnancy & Breastfeeding
  • Drug Images
  • Prochlorperazine Drug Interactions
  • Prochlorperazine Support Group
  • 13 Reviews for Prochlorperazine - Add your own review/rating


Compare Prochlorperazine with other medications


  • Anxiety
  • Hiccups
  • Nausea/Vomiting
  • Psychosis

Palonosetron Capsules


Pronunciation: PAL-oh-NOE-se-tron
Generic Name: Palonosetron
Brand Name: Aloxi


Palonosetron Capsules is used for:

Preventing nausea and vomiting caused by cancer chemotherapy. It may also be used for other conditions as determined by your doctor.


Palonosetron Capsules is 5-HT3 receptor blocker. It works by blocking the action of serotonin in certain parts of the brain and nervous system, which helps reduce or prevent nausea and vomiting.


Do NOT use Palonosetron Capsules if:


  • you are allergic to any ingredient in Palonosetron Capsules

  • you are taking apomorphine

Contact your doctor or health care provider right away if any of these apply to you.



Before using Palonosetron Capsules:


Some medical conditions may interact with Palonosetron Capsules. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you are allergic to other 5-HT3 receptor antagonists (eg, ondansetron)

  • if you have a history of heart problems (eg, irregular heartbeat, prolonged QT), an abnormal heart function test (eg, electrocardiogram [ECG]), or low blood levels of potassium or magnesium

Some MEDICINES MAY INTERACT with Palonosetron Capsules. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Apomorphine because side effects such as severely low blood pressure or loss of consciousness may occur

This may not be a complete list of all interactions that may occur. Ask your health care provider if Palonosetron Capsules may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Palonosetron Capsules:


Use Palonosetron Capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • An extra patient leaflet is available with Palonosetron Capsules. Talk to your pharmacist if you have questions about this information.

  • Take Palonosetron Capsules by mouth with or without food.

  • If you miss a dose of Palonosetron Capsules, contact your doctor right away.

Ask your health care provider any questions you may have about how to use Palonosetron Capsules.



Important safety information:


  • Palonosetron Capsules may cause dizziness. This effect may be worse if you take it with alcohol or certain medicines. Use Palonosetron Capsules with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Palonosetron Capsules should be used with extreme caution in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Palonosetron Capsules while you are pregnant. It is not known if Palonosetron Capsules is found in breast milk. Do not breast-feed while you are using Palonosetron Capsules.


Possible side effects of Palonosetron Capsules:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Constipation; headache; tiredness.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; fainting; fast, slow, or irregular heartbeat; fever, chills, or sore throat; trouble urinating; unusual muscle movement.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Palonosetron side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.


Proper storage of Palonosetron Capsules:

Store Palonosetron Capsules at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Palonosetron Capsules out of the reach of children and away from pets.


General information:


  • If you have any questions about Palonosetron Capsules, please talk with your doctor, pharmacist, or other health care provider.

  • Palonosetron Capsules is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Palonosetron Capsules. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Palonosetron resources


  • Palonosetron Side Effects (in more detail)
  • Palonosetron Dosage
  • Palonosetron Use in Pregnancy & Breastfeeding
  • Palonosetron Drug Interactions
  • Palonosetron Support Group
  • 0 Reviews for Palonosetron - Add your own review/rating


Compare Palonosetron with other medications


  • Nausea/Vomiting, Chemotherapy Induced
  • Nausea/Vomiting, Postoperative

Thursday, October 20, 2016

P Chlor DM


Generic Name: chlorpheniramine, dextromethorphan, and phenylephrine (klor feh NEER a meen, dex troe meh THOR fan, and feh nill EH frin)

Brand Names: Alka-Seltzer Plus Cold and Cough, C-Phen DM, C-Phen DM Drops, Cardec DM, Cardec DM Drops, Ceron-DM, Ceron-DM Drops, Cerose DM, Corfen-DM, CP Dec DM, CP Dec-DM Drops, De-Chlor DM, De-Chlor DR, Dec-Chlorphen DM, Dex PC, DM-PE-Chlor, Donatussin DM Drops, Ed A-Hist DM, HistadecDM, Maxiphen ADT, Mintuss DR, Nasohist-DM, Neo DM Drops, Nohist-DMX, Norel DM, P Chlor DM, PD-Cof, PD-Cof Drops, Poly-Tussin DM, Quartuss DM, Reme Tussin DM, Rondec-DM, Rondec-DM Drops, Rondex-DM, Rondex-DM Drops, Sildec-PE DM, Sildec-PE DM Drops, Tri-Vent DPC, Trital DM, Tussplex DM, Zotex-12D


What is P Chlor DM (chlorpheniramine, dextromethorphan, and phenylephrine)?

Chlorpheniramine is an antihistamine that reduces the natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.


Dextromethorphan is a cough suppressant. It affects the signals in the brain that trigger cough reflex.


Phenylephrine is a decongestant that shrinks blood vessels in the nasal passages. Dilated blood vessels can cause nasal congestion (stuffy nose).


Chlorpheniramine, dextromethorphan, and phenylephrine is used to treat sneezing, cough, runny or stuffy nose, itchy or watery eyes, hives, skin rash, itching, and other symptoms of allergies and the common cold.


Dextromethorphan will not treat a cough that is caused by smoking, asthma, or emphysema.


Chlorpheniramine, dextromethorphan, and phenylephrine may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about P Chlor DM (chlorpheniramine, dextromethorphan, and phenylephrine)?


Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children. Do not use a cough or cold medicine if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take cough or cold medicine before the MAO inhibitor has cleared from your body. Do not use any other over-the-counter cough, cold, allergy, or sleep medication without first asking your doctor or pharmacist. If you take certain products together you may accidentally take too much of one or more types of medicine. Read the label of any other medicine you are using to see if it contains an antihistamine, decongestant, or cough suppressant. Chlorpheniramine, dextromethorphan, and phenylephrine can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol. It can increase some of the side effects of this medication.

What should I discuss with my healthcare provider before taking P Chlor DM (chlorpheniramine, dextromethorphan, and phenylephrine)?


Do not use a cough or cold medicine if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take cough or cold medicine before the MAO inhibitor has cleared from your body.

Before taking this medication, tell your doctor if you are allergic to chlorpheniramine, dextromethorphan, or phenylephrine, or if you have:


  • kidney disease;

  • liver disease;


  • diabetes;




  • glaucoma;




  • heart disease or high blood pressure;




  • diabetes;




  • a thyroid disorder;




  • a stomach ulcer or a stomach obstruction,




  • emphysema or chronic bronchitis; or




  • an enlarged prostate or urination problems.



If you have any of these conditions, you may need a dose adjustment or special tests to safely take this medication.


FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Chlorpheniramine, dextromethorphan, and phenylephrine can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Artificially-sweetened liquid forms of cough-and-cold medications may contain phenylalanine. This would be important to know if you have phenylketonuria (PKU). Check the ingredients and warnings on the medication label if you are concerned about phenylalanine.


How should I take P Chlor DM (chlorpheniramine, dextromethorphan, and phenylephrine)?


Use this medication exactly as directed on the label or as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor.


Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children. Take this medicine with a full glass of water. If you use the effervescent tablet, drop the tablet in 8 ounces of water and allow it to dissolve completely. Stir this mixture and drink all of it right away. To make sure you get the entire dose, add a little more water to the same glass, swirl gently and drink right away.

Measure the liquid form of this medicine with a special dose-measuring spoon or cup, not a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist where you can get one.


Take this medicine with food or milk if it upsets your stomach.

This medication can cause you to have unusual results with allergy skin tests. Tell any doctor who treats you that you are taking an antihistamine.


Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash.

If you need to have any type of surgery, tell the surgeon ahead of time if you have taken a cold medicine within the past few days.


Store the medication at room temperature away from moisture and heat.

What happens if I miss a dose?


Since cough or cold medicine is usually taken only as needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regularly scheduled time. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include feeling restless or nervous, nausea, vomiting, stomach pain, dizziness, drowsiness, dry mouth, warmth or tingly feeling, or seizure (convulsions).


What should I avoid while taking P Chlor DM (chlorpheniramine, dextromethorphan, and phenylephrine)?


This medication can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol. It can increase some of the side effects of this medication. Before taking this medication, tell your doctor if you regularly use other medicines that make you sleepy (such as cold or allergy medicine, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for seizures, depression, or anxiety). They can add to sleepiness caused by this medication.

Avoid taking diet pills, caffeine pills, or other stimulants (such as ADHD medications) without your doctor's advice. Taking a stimulant together with a decongestant can increase your risk of unpleasant side effects.


Do not use any other over-the-counter cough, cold, allergy, or sleep medication without first asking your doctor or pharmacist. Antihistamines, decongestants, and cough suppressants are contained in many medicines available over the counter. If you take certain products together you may accidentally take too much of one or more types of medicine. Read the label of any other medicine you are using to see if it contains an antihistamine, decongestant, or cough suppressant.

P Chlor DM (chlorpheniramine, dextromethorphan, and phenylephrine) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using this medication and call your doctor at once if you have any of these serious side effects:

  • fast, pounding, or uneven heartbeat;




  • confusion, hallucinations, unusual thoughts or behavior;




  • severe dizziness, anxiety, restless feeling, or nervousness;




  • increased blood pressure (severe headache, blurred vision, trouble concentrating, chest pain, numbness, seizure);




  • confusion, hallucinations;




  • slow, shallow breathing;




  • urinating less than usual or not at all;




  • easy bruising or bleeding, unusual weakness, fever, chills, body aches, flu symptoms; or




  • nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes).



Less serious side effects may include:



  • blurred vision;




  • dry mouth;




  • nausea, stomach pain, constipation;




  • mild loss of appetite, stomach upset;




  • warmth, tingling, or redness under your skin;




  • feeling excited or restless;




  • sleep problems (insomnia);




  • restless or excitability (especially in children);




  • skin rash or itching;




  • dizziness, drowsiness;




  • problems with memory or concentration; or




  • ringing in your ears.



This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect P Chlor DM (chlorpheniramine, dextromethorphan, and phenylephrine)?


Before taking this medication, tell your doctor if you are using any of the following drugs:



  • an antidepressant;




  • a diuretic (water pill);




  • medication to treat irritable bowel syndrome;




  • celecoxib (Celebrex);




  • cinacalcet (Sensipar);




  • imatinib (Gleevec);




  • quinidine (Quinaglute, Quinidex);




  • ranolazine (Ranexa)




  • ritonavir (Norvir);




  • sibutramine (Meridia);




  • terbinafine (Lamisil);




  • medicines to treat high blood pressure;




  • aspirin or salicylates (such as Disalcid, Doan's Pills, Dolobid, Salflex, Tricosal, and others);




  • bladder or urinary medications such as darifenacin (Enablex), oxybutynin (Ditropan, Oxytrol) or tolterodine (Detrol); or




  • a beta-blocker such as atenolol (Tenormin), carteolol (Cartrol), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal), sotalol (Betapace), timolol (Blocadren), and others.



This list is not complete and there may be other drugs that can interact with chlorpheniramine, dextromethorphan, and phenylephrine. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.



More P Chlor DM resources


  • P Chlor DM Side Effects (in more detail)
  • P Chlor DM Use in Pregnancy & Breastfeeding
  • P Chlor DM Drug Interactions
  • P Chlor DM Support Group
  • 0 Reviews for P Chlor DM - Add your own review/rating


  • Bronkids Drops MedFacts Consumer Leaflet (Wolters Kluwer)

  • Cardec DM Elixir MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ceron-DM Liquid MedFacts Consumer Leaflet (Wolters Kluwer)

  • Maxiphen ADT MedFacts Consumer Leaflet (Wolters Kluwer)

  • Quartuss DM Prescribing Information (FDA)

  • Trital DM Prescribing Information (FDA)



Compare P Chlor DM with other medications


  • Cough and Nasal Congestion


Where can I get more information?


  • Your pharmacist can provide more information about chlorpheniramine, dextromethorphan, and phenylephrine.

See also: P Chlor DM side effects (in more detail)


Lamictal D.A.C.




Lamictal D.A.C. may be available in the countries listed below.


Ingredient matches for Lamictal D.A.C.



Lamotrigine

Lamotrigine is reported as an ingredient of Lamictal D.A.C. in the following countries:


  • Iceland

International Drug Name Search

Cetirizina Alter




Cetirizina Alter may be available in the countries listed below.


Ingredient matches for Cetirizina Alter



Cetirizine

Cetirizine dihydrochloride (a derivative of Cetirizine) is reported as an ingredient of Cetirizina Alter in the following countries:


  • Italy

  • Portugal

  • Spain

International Drug Name Search

Wednesday, October 19, 2016

Benzatina Bencilpenicilina




Benzatina Bencilpenicilina may be available in the countries listed below.


Ingredient matches for Benzatina Bencilpenicilina



Benzylpenicillin

Benzylpenicillin benzathine (a derivative of Benzylpenicillin) is reported as an ingredient of Benzatina Bencilpenicilina in the following countries:


  • Peru

International Drug Name Search

Previfem


Generic Name: ethinyl estradiol and norgestimate (ETH in ill ess tra DYE ol and nor JESS ti mate)

Brand Names: Mononessa, Ortho Tri-Cyclen, Ortho Tri-Cyclen Lo, Ortho-Cyclen, Previfem, Sprintec, Tri-Lo-Sprintec, Tri-Previfem, Tri-Sprintec, TriNessa


What is Previfem (ethinyl estradiol and norgestimate)?

Ethinyl estradiol and norgestimate contains a combination of female hormones that prevent ovulation (the release of an egg from an ovary). This medication also causes changes in your cervical mucus and uterine lining, making it harder for sperm to reach the uterus and harder for a fertilized egg to attach to the uterus.


Ethinyl estradiol and norgestimate is used as contraception to prevent pregnancy. It is also used to treat severe acne.


Ethinyl estradiol and norgestimate may also be used for purposes not listed in this medication guide.


What is the most important information I should know about Previfem (ethinyl estradiol and norgestimate)?


This medication can harm an unborn baby or cause birth defects. Do not use birth control pills if you are pregnant or if you have recently had a baby. You should not take birth control pills if you have coronary artery disease, severe heart valve disorder, uncontrolled high blood pressure, a history of stroke or blood clot, circulation problems, a hormone-related cancer such as breast or uterine cancer, unusual vaginal bleeding, liver disease or liver cancer, severe migraine headaches, or a history of jaundice caused by pregnancy or birth control pills.

You may need to use back-up birth control, such as condoms or a spermicide, when you first start using this medication. Follow your doctor's instructions.


Taking hormones can increase your risk of blood clots, stroke, or heart attack, especially if you smoke and are older than 35.

Some drugs can make birth control pills less effective, which may result in pregnancy. Tell your doctor about all the prescription and over-the-counter medications you use, including vitamins, minerals and herbal products. Do not start using a new medication without telling your doctor.


What should I discuss with my healthcare provider before taking Previfem (ethinyl estradiol and norgestimate)?


This medication can cause birth defects. Do not use if you are pregnant. Tell your doctor right away if you become pregnant, or if you miss two menstrual periods in a row. If you have recently had a baby, wait at least 4 weeks before taking birth control pills (6 weeks if you are breast-feeding). You should not take birth control pills if you have:

  • coronary artery disease, a severe or uncontrolled heart valve disorder, untreated or uncontrolled high blood pressure;




  • a history of a stroke, blood clot, or circulation problems;




  • a hormone-related cancer such as breast or uterine cancer;




  • unusual vaginal bleeding that has not been checked by a doctor;




  • liver disease or liver cancer;




  • severe migraine headaches; or




  • a history of jaundice caused by pregnancy or birth control pills.



To make sure you can safely take this medication, tell your doctor if you have any of these other conditions:



  • high blood pressure, heart disease, congestive heart failure, angina (chest pain), or a history of heart attack;




  • high cholesterol or triglycerides, or if you are overweight;




  • a history of depression;




  • gallbladder disease;




  • diabetes;




  • seizures or epilepsy;




  • a history of irregular menstrual cycles; or




  • a history of fibrocystic breast disease, lumps, nodules, or an abnormal mammogram.




The hormones in this medication can pass into breast milk and may harm a nursing baby. This medication may also slow breast milk production. Do not use if you are breast-feeding a baby.

How should I take Previfem (ethinyl estradiol and norgestimate)?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label. Take your first pill on the first day of your period or on the first Sunday after your period begins (follow your doctor's instructions).


You may need to use back-up birth control, such as condoms or a spermicide, when you first start using this medication. Follow your doctor's instructions.


The 28-day birth control pack contains seven "reminder" pills to keep you on your regular cycle. Your period will usually begin while you are using these reminder pills.


You may have breakthrough bleeding, especially during the first 3 months. Tell your doctor if this bleeding continues or is very heavy.

Take one pill every day, no more than 24 hours apart. When the pills run out, start a new pack the following day. You may get pregnant if you do not use this medication regularly. Get your prescription refilled before you run out of pills completely.


If you need surgery or medical tests or if you will be on bed rest, you may need to stop using this medication for a short time. Any doctor or surgeon who treats you should know that you are using birth control pills.


Your doctor will need to check your progress on a regular basis. Do not miss any scheduled appointments.


Store at room temperature away from moisture and heat.

What happens if I miss a dose?


Missing a pill increases your risk of becoming pregnant.


If you miss one "active" pill, take two pills on the day that you remember. Then take one pill per day for the rest of the pack.


If you miss two "active" pills in a row in week one or two, take two pills per day for two days in a row. Then take one pill per day for the rest of the pack. Use back-up birth control for at least 7 days.


If you miss two "active" pills in a row in week three, or if you miss three pills in a row during any of the first 3 weeks, throw out the rest of the pack and start a new one the same day if you are a Day 1 starter. If you are a Sunday starter, keep taking a pill every day until Sunday. On Sunday, throw out the rest of the pack and start a new one that day.


If you miss two or more pills, you may not have a period during the month. If you miss a period for two months in a row, call your doctor because you might be pregnant.

If you miss any reminder pills, throw them away and keep taking one pill per day until the pack is empty. You do not need back-up birth control if you miss a reminder pill.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. Overdose symptoms may include severe nausea or vaginal bleeding.

What should I avoid while taking Previfem (ethinyl estradiol and norgestimate)?


Do not smoke while using birth control pills, especially if you are older than 35. Smoking can increase your risk of blood clots, stroke, or heart attack caused by birth control pills.

Birth control pills will not protect you from sexually transmitted diseases--including HIV and AIDS. Using a condom is the only way to protect yourself from these diseases.


Previfem (ethinyl estradiol and norgestimate) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop taking this medicine and call your doctor at once if you have a serious side effect such as:

  • sudden numbness or weakness, especially on one side of the body;




  • sudden severe headache, confusion, problems with vision, speech, or balance;




  • sudden cough, wheezing, rapid breathing, coughing up blood;




  • pain, swelling, warmth, or redness in one or both legs;




  • chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;




  • a change in the pattern or severity of migraine headaches;




  • pain in your upper stomach, jaundice (yellowing of the skin or eyes);




  • a lump in your breast;




  • swelling in your hands, ankles, or feet; or




  • symptoms of depression (sleep problems, weakness, mood changes).



Less serious side effects may include:



  • mild nausea or vomiting, appetite or weight changes;




  • breast swelling or tenderness;




  • headache, nervousness, dizziness;




  • problems with contact lenses;




  • freckles or darkening of facial skin, loss of scalp hair; or




  • vaginal itching or discharge.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Previfem (ethinyl estradiol and norgestimate)?


Some drugs can make ethinyl estradiol and norgestimate less effective, which may result in pregnancy. Before using ethinyl estradiol and norgestimate, tell your doctor if you are using any of the following drugs:



  • bosentan (Tracleer);




  • St. John's wort;




  • an antibiotic;




  • HIV or AIDS medications;




  • phenobarbital (Solfoton) and other barbiturates; or




  • seizure medication.



This list is not complete and other drugs may interact with birth control pills. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Previfem resources


  • Previfem Side Effects (in more detail)
  • Previfem Use in Pregnancy & Breastfeeding
  • Drug Images
  • Previfem Drug Interactions
  • Previfem Support Group
  • 0 Reviews for Previfem - Add your own review/rating


  • Previfem Prescribing Information (FDA)

  • MonoNessa Prescribing Information (FDA)

  • Ortho Tri-Cyclen MedFacts Consumer Leaflet (Wolters Kluwer)

  • Ortho Tri-Cyclen Consumer Overview

  • Ortho Tri-Cyclen Prescribing Information (FDA)

  • Ortho Tri-Cyclen Lo Prescribing Information (FDA)

  • Sprintec Prescribing Information (FDA)

  • Tri-Lo-Sprintec Prescribing Information (FDA)

  • Tri-Previfem Prescribing Information (FDA)

  • Tri-Sprintec Prescribing Information (FDA)

  • TriNessa Prescribing Information (FDA)



Compare Previfem with other medications


  • Abnormal Uterine Bleeding
  • Birth Control
  • Endometriosis
  • Gonadotropin Inhibition
  • Ovarian Cysts


Where can I get more information?


  • Your pharmacist can provide more information about ethinyl estradiol and norgestimate.

See also: Previfem side effects (in more detail)