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


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  • Gentamicin Drug Interactions
  • Gentamicin Support Group
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  • 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.