Generic Name: Prometrium
What is Prometrium?
Standard Shipping Fee Per Order The lowest fee that the online pharmacy offers. This is usually the standard mail fee. Some fees may be conditional upon minimum orders - for more information see the "Other Shipping Options" section in the pharmacy's Profile. Need to Send Your Original Prescription. The pharmacy requires a prescription to fill your order. This is generally in your best interest to be sure that a prescription is appropriate for you.
For most pharmacies, you need to send the prescription your doctor gave you. Some foreign pharmacies, such as many in Canada, will have a local physician re-write the prescription so that it can be legally filled.
PROGRAF can cause serious side effects, including:Do not take PROGRAF if you are allergic to tacrolimus or any of the ingredients in PROGRAF. What should I tell my doctor before taking PROGRAF. Before you take PROGRAF, tell your doctor if you: plan to receive any live vaccines, have or have had liver, kidney or heart problems, are pregnant or plan to become pregnant. Talk to your doctor if you are pregnant or plan to become pregnant. Tell your doctor if you are breastfeeding or plan to breastfeed.
PROGRAF can pass into your breast milk. You and your doctor should decide if you will take PROGRAF or breastfeed. You should not do both. Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements.
How should I take Prometrium?
Missed Doses If your child misses a dose of tacrolimus, call your coordinator for advice. Side Effects Common side effects include: Increased risk of infection. Burning or tingling of the mouth, hands, or feet. Contact your coordinator for any undiagnosed headache that lasts more than 24 hours or is accompanied by a fever or a stiff neck. Hyperglycemia high blood sugar.
What should I avoid while taking Prometrium?
Conversion from ciclosporin Care should be taken when converting patients from ciclosporin-based to Prograf-based therapy see sections 4. Target whole blood trough concentration recommendations Dosing should primarily be based on clinical assessments of rejection and tolerability in each individual patient. Hypersensitivity to tacrolimus or other macrolides. Medication errors, including inadvertent, unintentional or unsupervised substitution of immediate- or prolonged-release tacrolimus formulations, have been observed.
Lymphoproliferative disorders and malignancies Patients treated with Prograf have been reported to develop Epstein-Barr Virus EBV -associated lymphoproliferative disorders see section 4.
Inhibitors of metabolism Clinically the following substances have been shown to increase tacrolimus blood levels:Strong interactions have been observed with antifungal agents such as ketoconazole, fluconazole, itraconazole and voriconazole, the macrolide antibiotic erythromycin, HIV protease inhibitors e.
Prometrium side effects
Target whole blood trough concentration recommendationsDosing should primarily be based on clinical assessments of rejection and tolerability in each individual patient. As an aid to optimise dosing, several immunoassays are available for determining tacrolimus concentrations in whole blood including a semi-automated microparticle enzyme immunoassay MEIA. Comparisons of concentrations from the published literature to individual values in clinical practice should be assessed with care and knowledge of the assay methods employed.
In current clinical practice, whole blood levels are monitored using immunoassay methods. Blood trough levels of tacrolimus should be monitored during the post-transplantation period. When dosed orally, blood trough levels should be drawn approximately 12 hours post-dosing, just prior to the next dose.
Common Prometrium ide effects may include:
Your doctor may do certain tests to check your kidney function.
John's Wort, Hypericum perforatum: St.
Additionally, both tacrolimus and mefloquine are CYP3A4 substrates.
In a study comparing tacrolimus and cyclosporine, 11 pediatric patients ages 3-18 years received an initial tacrolimus dose of 0.
The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for you or anyone else.
A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.
Where can I get more information?
The potential for proarrhythmic events with ibutilide increases with the coadministration of other drugs that prolong the QT interval.
Although causality for TdP has not been established for flecainide, patients receiving concurrent drugs which have the potential for QT prolongation may have an increased risk of developing proarrhythmias.