Sunday 18 January 2009

Iruxol mono




Iruxol mono may be available in the countries listed below.


Ingredient matches for Iruxol mono



Collagenase

Collagenase is reported as an ingredient of Iruxol mono in the following countries:


  • Austria

  • Finland

  • Greece

  • Netherlands

  • South Africa

  • Spain

  • Switzerland

International Drug Name Search

Saturday 17 January 2009

Dexametasona Lacefa




Dexametasona Lacefa may be available in the countries listed below.


Ingredient matches for Dexametasona Lacefa



Dexamethasone

Dexamethasone is reported as an ingredient of Dexametasona Lacefa in the following countries:


  • Argentina

International Drug Name Search

Dasatinib




In the US, Dasatinib (dasatinib systemic) is a member of the drug class BCR-ABL tyrosine kinase inhibitors and is used to treat Acute Lymphoblastic Leukemia, Chronic Myelogenous Leukemia and Leukemia.

US matches:

  • Dasatinib

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

L01XE06

CAS registry number (Chemical Abstracts Service)

0302962-49-8

Chemical Formula

C22-H26-Cl-N7-O2-S

Molecular Weight

488

Therapeutic Category

Antineoplastic agent

Chemical Names

N-(2-chloro-6-methylphenyl)-2-({6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl}amino)-1,3-thiazole-5-carboxamide (WHO)

2-{6-[4-(2-Hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-ylamino}thiazol-5-carbonsäure-(2-chlor-6-methylphenyl)amid (IUPAC)

5-Thiazolecarboxamide-N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-

Foreign Names

  • Dasatinibum (Latin)
  • Dasatinib (German)
  • Dasatinib (French)
  • Dasatinib (Spanish)

Generic Names

  • BMS 354825 (IS: Bristol-Myers)
  • Dasatinib (OS: USAN)
  • BMS-354825-03 (IS)
  • UNIIRBZ157X5H (IS)

Brand Names

  • Sprycel
    Bristol-Myers Squibb, Australia; Bristol-Myers Squibb, Canada; Bristol-Myers Squibb, Switzerland; Bristol-Myers Squibb, Denmark; Bristol-Myers Squibb, Indonesia; Bristol-Myers Squibb, New Zealand; Bristol-Myers Squibb, Poland; Bristol-Myers Squibb, Slovenia; Bristol-Myers Squibb, Argentina; Bristol-Myers Squibb, Austria; Bristol-Myers Squibb, Belgium; Bristol-Myers Squibb, Switzerland; Bristol-Myers Squibb, Czech Republic; Bristol-Myers Squibb, Germany; Bristol-Myers Squibb, Spain; Bristol-Myers Squibb, France; Bristol-Myers Squibb, United Kingdom; Bristol-Myers Squibb, Hungary; Bristol-Myers Squibb, Ireland; Bristol-Myers Squibb, Italy; Bristol-Myers Squibb, Japan; Bristol-Myers Squibb, Netherlands; Bristol-Myers Squibb, Norway; Bristol-Myers Squibb, Oman; Bristol-Myers Squibb, Sweden; Bristol-Myers Squibb, United States; Bristol-Myers Squibb Phar, Luxembourg

International Drug Name Search

Glossary

IUPACInternational Union of Pure and Applied Chemistry
ISInofficial Synonym
OSOfficial Synonym
Rec.INNRecommended International Nonproprietary Name (World Health Organization)
USANUnited States Adopted Name
WHOWorld Health Organization

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

Monday 12 January 2009

Optiray 240


Generic Name: ioversol (eye oh VERS ol)

Brand Names: Optiray 160, Optiray 240, Optiray 300, Optiray 320, Optiray 350


What is Optiray 240 (ioversol)?

Ioversol is in a group of drugs called radiopaque (RAY dee oh payk) contrast agents. Ioversol contains iodine, a substance that absorbs x-rays. Radiopaque contrast agents are used to allow blood vessels, organs, and other non-bony tissues to be seen more clearly on a CT scan or other radiologic (x-ray) examination.


Ioversol is used to help diagnose certain disorders of the heart, brain, and blood vessels.


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


What is the most important information I should know about Optiray 240 (ioversol)?


You should not receive ioversol if you have any type of active infection.

Tell your doctor if you have asthma, hay fever, or history of food or drug allergies, especially if you have had any type of reaction to another contrast agent.


Drink extra fluids before and after you receive ioversol. This medication can cause you to get dehydrated, which can lead to dangerous effects on your kidneys. Follow your doctor's instructions about the types and amount of fluids you should drink before and after your test.

What should I discuss with my health care provider before receiving Optiray 240 (ioversol)?


Tell your doctor if you have ever had any type of reaction to another contrast agent.


You should not receive ioversol if you have any type of active infection.

Before receiving ioversol, tell your doctor if you have:



  • a brain tumor or hematoma;




  • a recent head or brain injury;




  • epilepsy or other seizure disorder;




  • a bleeding or blood clotting disorder;




  • kidney disease;




  • liver disease;




  • diabetes;




  • heart disease, angina, or congestive heart failure;




  • homocysteinuria;




  • sickle cell disease;




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




  • asthma, hay fever, or a history of food or drug allergies;




  • multiple myeloma (bone cancer);




  • pheochromocytoma; or




  • a thyroid disorder.



If you have any of these conditions, you may not be able to receive ioversol, or you may need a dosage adjustment or special tests during treatment.


FDA pregnancy category B. This medication is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether ioversol passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Older adults may need special care in avoiding dehydration by drinking extra fluids before and after the radiologic test. Your kidney function may also need to be watched closely after you have received ioversol.


How is ioversol used?


Ioversol is given as an injection through a needle placed into a vein. You will receive this injection in a clinic or hospital setting during your radiologic test.


Drink extra fluids before and after you receive ioversol. This medication can cause you to get dehydrated, which can lead to dangerous effects on your kidneys. Follow your doctor's instructions about the types and amount of fluids you should drink before and after your test. Your doctor or other healthcare provider may want to watch you for a short period of time after your injection. This is to make sure you do not have any unwanted side effects or delayed reactions.

This medication can cause you to have unusual results with certain thyroid tests. If you have such tests within 16 days after receiving ioversol, tell the doctor in charge that you have recently received ioversol.


What happens if I miss a dose?


Since ioversol is used only during your radiologic test, you will not be on a dosing schedule.


What happens if I overdose?


Seek emergency medical attention if you think you have received too much of this medicine. Symptoms of an ioversol overdose may include chest pain, trouble breathing, and slow or uneven heartbeats.

What should I avoid while receiving Optiray 240 (ioversol)?


Do not allow yourself to become dehydrated during the first few days after receiving ioversol. Call your doctor if you have any vomiting or diarrhea during this time. Follow your doctor's instructions about the types and amount of fluids you should drink.

Optiray 240 (ioversol) side effects


Some of the side effects of ioversol can occur up to 24 hours after you have received the medication.


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 at once if you have any of these serious side effects:

  • urinating less than usual or not at all;




  • severe muscle pain or weakness;




  • seizure (convulsions);




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




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




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




  • feeling light-headed, fainting;




  • wheezing, trouble breathing;




  • fast or slow heartbeat;




  • easy bruising, unusual bleeding, or skin changes; or




  • swelling of your hands, ankles, or feet.



Other less serious side effects are more likely to occur, such as:



  • fever, warmth, or pain;




  • skin rash or redness;




  • headache; or




  • nausea.



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 Optiray 240 (ioversol)?


There may be other drugs that can affect ioversol. 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 Optiray 240 resources


  • Optiray 240 Side Effects (in more detail)
  • Optiray 240 Use in Pregnancy & Breastfeeding
  • Optiray 240 Drug Interactions
  • Optiray 240 Support Group
  • 0 Reviews for Optiray 240 - Add your own review/rating


Compare Optiray 240 with other medications


  • Body Imaging
  • Cerebral Arteriography
  • Coronary Arteriography
  • Head Imaging
  • Intra-arterial Digital Subtraction Angiography
  • Intravenous Digital Subtraction Angiography
  • Intravenous Urography
  • Left Ventriculography
  • Pediatric Angiocardiography
  • Peripheral Arteriography
  • Renal Arteriography
  • Venography
  • Visceral Arteriography


Where can I get more information?


  • Your doctor or pharmacist has more information about ioversol written for health professionals that you may read.

See also: Optiray 240 side effects (in more detail)


Norglicem 5




Norglicem 5 may be available in the countries listed below.


Ingredient matches for Norglicem 5



Glibenclamide

Glibenclamide is reported as an ingredient of Norglicem 5 in the following countries:


  • Spain

International Drug Name Search

Saturday 10 January 2009

Dipyridamol Sandoz




Dipyridamol Sandoz may be available in the countries listed below.


Ingredient matches for Dipyridamol Sandoz



Dipyridamole

Dipyridamole is reported as an ingredient of Dipyridamol Sandoz in the following countries:


  • Netherlands

International Drug Name Search

Thursday 8 January 2009

Ortho Evra Patch


Pronunciation: nor-el-JES-troe-min/ETH-i-nil ES-tra-DYE-ol
Generic Name: Norelgestromin/Ethinyl Estradiol
Brand Name: Ortho Evra

Smoking cigarettes while using Ortho Evra Patch increases the risk of serious heart problems. The risk increases with age (older than 35 years) and with frequent smoking. Patients who use Ortho Evra Patch are strongly advised not to smoke. Do not use Ortho Evra Patch if you are older than 35 years and you smoke.


Women who use Ortho Evra Patch may have a higher risk of developing serious blood clots than women who use birth control pills. Discuss any questions or concerns with your doctor.





Ortho Evra Patch is used for:

Preventing pregnancy. It may also be used for other conditions as determined by your doctor.


Ortho Evra Patch is an estrogen/progestin combination. It works by preventing the release of eggs from the ovaries and thereby preventing pregnancy.


Do NOT use Ortho Evra Patch if:


  • you are allergic to any ingredient in Ortho Evra Patch

  • you are pregnant or suspect you may be pregnant, have recently given birth, or are breast-feeding

  • you have blood clots in the legs, lungs, or eyes, or a history of other blood clotting problems

  • you have a history of blood vessel problems of the heart or brain, a heart attack, chest pain, or a stroke

  • you have a history of yellowing of the eyes or skin during pregnancy or previous hormonal birth control use

  • you have a history of breast cancer; or known or suspected breast cancer or cancer of the uterus, cervix, or vagina; cancer that is estrogen-dependent; or you have unusual vaginal bleeding from an unknown cause

  • you have a liver tumor, liver cancer, or active liver disease; severe high blood pressure; blood vessel problems caused by diabetes; certain heart valve problems; or the blood disease porphyria

  • you have headaches with neurological symptoms or will be on bed rest for a long period following surgery

  • you are taking birth control pills

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



Before using Ortho Evra Patch:


Some medical conditions may interact with Ortho Evra Patch. 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 high blood pressure; high cholesterol, triglycerides, or calcium levels; or pancreatitis or gallbladder problems; or you are obese

  • if you have breast nodules, fibrocystic disease of the breast, an abnormal breast x-ray or mammogram, endometriosis or endometrial carcinomas, uterine fibroids, or irregular or scanty menstrual periods

  • if a member of your family has had breast cancer

  • if you have liver or kidney problems, heart problems, diabetes, headaches, migraine headaches, epilepsy, or a history of mental depression

  • if you smoke, weigh 198 lbs or more, or will be having surgery

  • if you have recently given birth or had a miscarriage or abortion

  • if you are taking an antibiotic

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


  • Azole antifungals (eg, ketoconazole) or HMG-CoA reductase inhibitors (eg, atorvastatin) because they may increase the risk of Ortho Evra Patch's side effects

  • Aprepitant, azole antifungals (eg, itraconazole), barbiturates (eg, phenobarbital), bosentan, carbamazepine, felbamate, griseofulvin, HIV protease inhibitors (eg, ritonavir), hydantoins (eg, phenytoin), modafinil, nonnucleoside reverse transcriptase inhibitors (NNRTIs) (eg, nevirapine), oxcarbazepine, penicillins (eg, amoxicillin), rifampin, St. John's wort, tetracyclines (eg, doxycycline), topiramate, or troglitazone because they may decrease Ortho Evra Patch's effectiveness. Alternative forms of birth control are strongly recommended when taking any of these medicines along with this birth control medicine

  • Beta-blockers (eg, atenolol), corticosteroids (eg, prednisolone), selegiline, theophyllines (eg, aminophylline), or troleandomycin because the risk of their side effects may be increased by Ortho Evra Patch

  • Lamotrigine, morphine, or temazepam because their effectiveness may be decreased by Ortho Evra Patch

This may not be a complete list of all interactions that may occur. Ask your health care provider if Ortho Evra Patch 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 Ortho Evra Patch:


Use Ortho Evra Patch as directed by your doctor. Check the label on the medicine for exact dosing instructions.


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

  • One patch is usually applied to the skin, worn for 1 week, and then replaced. Follow the dosing schedule carefully.

  • Do not open the sealed pouch containing the patch until you are ready to use it. Open the pouch and remove the patch from the protective liner. Apply to an area of clean, dry skin on the lower stomach area below the belly button. Press the patch firmly against the skin for about 10 seconds to be sure the patch stays on. If the patch lifts, press down to reapply. Wear only 1 patch at any one time.

  • Do not place the patch on the breast. Make sure the application site is not oily, damaged, or irritated. Avoid applying to the waistline because tight clothing may rub the patch off. Do not put the patch on areas where sitting may loosen it. Do not apply to a site that is exposed to sunlight or where the skin is red, irritated, or cut. Do not use creams, oils, powder, or makeup on your skin where you will put a patch or near a patch you are using because it may cause the patch to become loose. Contact with water while bathing, showering, or swimming will not affect the patch.

  • When it is time to change the patch, remove it slowly. After removing the used patch, fold it in half with the sticky sides together. Discard the patch out of the reach of children and away from pets.

  • Apply a new patch to a different area to prevent skin irritation. Use a different site when replacing the patch and do not repeat the same site for at least 1 week. If the area around the patch becomes red, itchy, or irritated, remove that patch. Apply a new patch at a different site until your next scheduled patch change. If the irritation continues or becomes worse, notify your doctor promptly.

  • If the patch has become loose or has fallen off for less than 1 day, try to reapply it or apply a new patch immediately. No other contraceptive measures are necessary.

  • If the patch has become loose or has fallen off for more than 1 day or if you are not sure how long it has been off, apply a new patch to begin a new cycle. In this case, you may not be adequately protected from pregnancy. You must use an additional form of birth control (eg, diaphragm, male condoms, spermicide) until the patch has been in place for 7 days in a row.

  • Do not try to reapply a patch if it is no longer sticky, if it has become stuck to itself or another surface, if it has other material stuck to it, or if it has previously come loose or fallen off. Do not use any tapes or wraps to keep the patch in place. If you cannot reapply a patch, apply a new patch immediately.

  • Check with your doctor before you eat grapefruit or drink grapefruit juice while you use Ortho Evra Patch. Eating grapefruit or drinking grapefruit juice may increase the risk of Ortho Evra Patch's side effects.

  • If you forget to change your patch on the scheduled day, follow the directions in the additional patient leaflet that comes with Ortho Evra Patch. You may need to use a backup form of birth control (eg, condoms). If you forget to change your patch on the scheduled day and you are not sure what to do, use an extra form of birth control (eg, condoms) and check with your doctor or pharmacist.

Ask your health care provider any questions you may have about how to use Ortho Evra Patch.



Important safety information:


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

  • Limit alcoholic beverages.

  • Ortho Evra Patch may cause dark skin patches on your face (melasma). Avoid the sun, sunlamps, or tanning booths until you know how you react to Ortho Evra Patch. Use a sunscreen or wear protective clothing if you must be outside for more than a short time.

  • Ortho Evra Patch may increase the risk of stroke, heart attack, blood clots, high blood pressure, or similar problems. The risk may be greater if you smoke (especially in women older than 35 years).

  • The risk of developing a blood clot may be greater with Ortho Evra Patch than with other forms of hormonal birth control (eg, birth control pill). Talk with your doctor about the benefits and risks of Ortho Evra Patch or other forms of hormonal birth control.

  • Some antibiotics may decrease Ortho Evra Patch's effectiveness. If you take an antibiotic while you are using Ortho Evra Patch, talk with your doctor or pharmacist. You may need to use an additional form of birth control (eg, condoms) while you take the antibiotic. Discuss any questions or concerns with your doctor.

  • Contact your doctor if vaginal bleeding of unknown cause occurs. This could be a sign of a serious condition requiring immediate medical attention.

  • Contact your doctor if vaginal discomfort occurs or if you suspect you have developed an infection while using Ortho Evra Patch.

  • Follow your doctor's instructions for examining your breasts and report any lumps immediately.

  • If you wear contact lenses and you develop problems with them, contact your doctor.

  • If you will be having surgery or will be confined to a chair or bed for a long period of time (eg, a long plane flight), notify your doctor beforehand. Special precautions may need to be taken in these circumstances while you are using Ortho Evra Patch.

  • Nonprescription therapy to help prevent bone loss includes a weight-bearing exercise plan, as well as adequate daily calcium and vitamin D intake. Consult your doctor or pharmacist for more details.

  • Ortho Evra Patch may increase the risk of breast and endometrial cancer.

  • Ortho Evra Patch does not stop the spread of HIV and other sexually transmitted diseases (STDs). Use barrier methods of birth control (eg, condoms) if you have HIV infection or an STD. Do not share needles, injection supplies, or items like toothbrushes or razors.

  • Diabetes patients - Ortho Evra Patch may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Ortho Evra Patch may interfere with certain lab tests. Be sure your doctor and lab personnel know you are using Ortho Evra Patch.

  • Lab tests will be required to monitor therapy. You should have a complete physical examination, including blood pressure measurements, breast and pelvic examinations, and a Pap test, at least once a year. You should also have periodic mammograms as determined by your doctor. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Ortho Evra Patch is not approved for use in CHILDREN who have not yet had their first menstrual period; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: Do not use Ortho Evra Patch if you are pregnant. Avoid becoming pregnant while you are using it. If you miss a menstrual period or think you may be pregnant, contact your doctor right away. Ortho Evra Patch may be found in breast milk. If you are or will be breast-feeding while you use Ortho Evra Patch, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Ortho Evra Patch:


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:



Breast tenderness or enlargement; headache; menstrual cramps; mild skin irritation at the application site; nausea; stomach pain, cramps, or bloating; vaginal spotting or breakthrough bleeding; vomiting.



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); breast lumps; breast pain; calf pain, swelling, or tenderness; changes in vision (eg, double vision, loss of vision); chest pain; confusion; coughing up blood; fainting; mental or mood changes (eg, depression, memory loss); pain, swelling, or tenderness in the stomach; severe headache or vomiting; severe or persistent dizziness; severe or persistent trouble sleeping; severe or persistent vaginal bleeding; slurred speech; sudden shortness of breath; swelling of the hands or feet; symptoms of liver problems (eg, yellowing of the skin or eyes, fever, dark urine, pale stools, loss of appetite); unusual tiredness or weakness; unusual vaginal discharge, itching, or odor; weakness or numbness of an arm or leg.



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: Ortho Evra 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 excessive vaginal bleeding; severe nausea; vomiting.


Proper storage of Ortho Evra Patch:

Store Ortho Evra Patch at 77 degrees F (25 degrees C) in the original sealed pouch. 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 Ortho Evra Patch out of the reach of children and away from pets.


General information:


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

  • Ortho Evra Patch 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 Ortho Evra Patch. 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 Ortho Evra resources


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


Compare Ortho Evra with other medications


  • Birth Control

Sunday 4 January 2009

Myonit




Myonit may be available in the countries listed below.


Ingredient matches for Myonit



Nitroglycerin

Nitroglycerin is reported as an ingredient of Myonit in the following countries:


  • India

International Drug Name Search

Saturday 3 January 2009

Marperis




Marperis may be available in the countries listed below.


Ingredient matches for Marperis



Aluminium Hydroxide

Aluminium Hydroxide is reported as an ingredient of Marperis in the following countries:


  • Japan

Magnesium Hydroxide

Magnesium Hydroxide is reported as an ingredient of Marperis in the following countries:


  • Japan

International Drug Name Search

Diazepam NEGPF




Diazepam NEGPF may be available in the countries listed below.


Ingredient matches for Diazepam NEGPF



Diazepam

Diazepam is reported as an ingredient of Diazepam NEGPF in the following countries:


  • China

International Drug Name Search

Evacuol




Evacuol may be available in the countries listed below.


Ingredient matches for Evacuol



Sodium Phosphate

Sodium Phosphate Monobasic dihydrate and Dibasic dodecahydrate (a derivative of Sodium Phosphate) is reported as an ingredient of Evacuol in the following countries:


  • Peru

Sodium Picosulfate

Sodium Picosulfate is reported as an ingredient of Evacuol in the following countries:


  • Spain

International Drug Name Search