< The possibility of interactions with other drugs administered concurrently should be considered, particularly when their main route of elimination is active renal secretion via the organic cationic transport system (e.g., trimethoprim) Coadministration of single doses of Lamivudine and sorbitol resulted in a sorbitol dose-dependent reduction in Lamivudine exposures. © 2012Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 101:2143–2154, 2012We use cookies to help provide and enhance our service and tailor content and ads. Lamivudine, also known as epivir or 3TC, belongs to the class of organic compounds known as 3'-thia pyrimidine nucleosides. 0000006435 00000 n Avoid doing things that can spread HBV infection to others.What should I tell my healthcare provider before taking Lamivudine tablets (HBV)?Before taking Lamivudine tablets (HBV), tell your healthcare provider about all of your medical conditions, including if you:Tell your healthcare provider about all the medicines you take,Keep a list of your medicines to show your healthcare provider and pharmacist.Do not start taking a new medicine without telling your healthcare provider.Lamivudine tablets (HBV) should not be taken if you also take other medicines that contain Lamivudine or emtricitabine.What are the possible side effects of Lamivudine tablets (HBV)?Lamivudine tablets (HBV) may cause serious side effects, including:Call your healthcare provider right away if you get any of the following symptoms that could be signs of lactic acidosis:Call your healthcare provider right away if you get any of the following signs or symptoms of liver problems:You may be more likely to get lactic acidosis or severe liver problems if you are female or very overweight (obese).The most common side effects of Lamivudine tablets (HBV) includeKeep Lamivudine tablets (HBV) and all medicines out of the reach of children.What are the ingredients in Lamivudine tablets (HBV)?We comply with the HONcode standard for trustworthy health information - Data sources include IBM Watson Micromedex (updated 2 Sep 2020), Cerner Multum™ (updated 1 Sep 2020), … solubility, lamivudine is classified as Class III compound (9). 0000006021 00000 n 0000007299 00000 n Histologic Response at Week 52 among Adult Subjects Receiving Lamivudine Tablets (HBV) 100 mg Once Daily or PlaceboAdvise the patient to read the FDA-approved patient labeling (Patient Information).Severe Acute Exacerbation of Hepatitis after Discontinuation of TreatmentRisk of Development of HIV-1 Resistance in Patients with HIV-1 Co-infectionWhat is the most important information I should know about Lamivudine tablets (HBV)?• Risk of HIV-1 resistance in people with unknown HIV-1 infection or in people with untreated HIV-1 infection.Lamivudine tablets (HBV) does not stop you from spreading HBV to others by sex, sharing needles, or being exposed to your blood. Lamivudine drug products fulfill the criterion of very rapidly dissolving (more than 85% of the labeled amount of the drug dissolved within 15 min in each required medium).
The makers of these brands are not affiliated with and do not endorse Annora Pharma Private Limited or its products.Lamivudine Tablets, USP (HBV) 100 mg - 60s container LabelThe easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Lamivudine has been used to deplete the Hepatitis B Virus (HBV) covalently closed circular DNA (cccDNA) forms for the preparation of inverse nested PCR. 0000000736 00000 n 0000002552 00000 n 2006 Sep 14;321(1-2):101-7. doi: 10.1016/j.ijpharm.2006.05.013. Such observations should be taken into consideration when determining the advisability of continuing therapy with Lamivudine tablets (HBV).• Lamivudine tablets USP (HBV): 100 mg are white, capsule shaped biconvex, film coated, tablets debossed with '1' on one side and 'V' on the other side.Lamivudine tablets (HBV) are contraindicated in patients with a previous hypersensitivity reaction to Lamivudine.Clinical and laboratory evidence of exacerbations of hepatitis have occurred after discontinuation of Lamivudine.
Pharmacokinetic Parameters (Mean ± SD) Dose-Normalized to a Single 100-mg Dose of Lamivudine in Adults with Normal or Impaired Hepatic FunctionEffect of Lamivudine on the Pharmacokinetics of Other Agents:Effect of Other Agents on the Pharmacokinetics of LamivudineTable 7.
Because a negligible amount of Lamivudine was removed via (4-hour) hemodialysis, continuous ambulatory peritoneal dialysis, and automated peritoneal dialysis, it is not known if continuous hemodialysis would provide clinical benefit in a Lamivudine overdose event.Lamivudine tablet, USP (HBV) is a synthetic nucleoside analogue with activity against HBV. Elsevier Science These are nucleoside analogues with a structure that consists of a pyrimidine base, which is N-substituted at the 1-position with a 3'-thia derivative (1, 3-oxazolidine) of the ribose moiety that is characteristic of nucleosides. 0000002034 00000 n Here, water solubilities of lamivudine hydrochloride, lamivudine hydrochloride monohydrate, and lamivudine duplex are reported.
Epub 2015 Mar 11.Int J Pharm.
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