MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. 1-888-info-fda (1-888-463-6332) Contact FDA Subscribe to FDA RSS feeds Follow FDA on Twitter Follow FDA on Facebook View FDA videos on YouTube View FDA photos on Flickr FDA Home; Drugs; Drug Approvals and Databases; Drugs@FDA - Sustiva (efavirenz), 50mg, 100mg, 200mg capsules Company: DuPont Pharmaceuticals Company Application No. Unintentional dosing of Torsemide, 20mg Tablets could cause excessive urination. Original Approvals or Tentative Approvals. Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url; 12/22/1989: ORIG-1: Approval Type 3 - New Dosage Form … Available for Android and iOS devices.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these drug products.Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:Gavreto (pralsetinib) is an oral selective RET kinase inhibitor for the...Detectnet (copper Cu 64 dotatate) is a radioactive diagnostic agent indicated...Onureg (azacitidine) is a nucleoside metabolic inhibitor indicated for the...Qdolo (tramadol hydrochloride) is an opioid agonist indicated in adults for ...The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Following is a list of possible medication recalls, market withdrawals, alerts and warnings. Select one or more newsletters to continue. … We comply with the HONcode standard for trustworthy health information - Home; Food; Drugs; Medical Devices; Radiation-Emitting Products; Vaccines, Blood & Biologics; Animal & Veterinary; Cosmetics; Tobacco Products . Following is a list of possible medication recalls, market withdrawals, alerts and warnings. The FDA Alert(s) below may be specifically about Sustiva or relate to a group or class of drugs which include Sustiva (efavirenz). Herpetic keratitis is an infection of the cornea that is caused by the herpes simplex virus. For the latest FDA MedWatch alerts, go here. Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url; 10/29/2019: SUPPL-57: Labeling-Package Insert, Labeling-Patient Package Insert acyclovir FDA Alerts. Acyclovir is a synthetic nucleoside analogue active against herpesviruses. We comply with the HONcode standard for trustworthy health information - Drug Approval Package. In addition, each tablet contains the inactive ingredients colloidal silicon dioxide, magnesium stearate, microcrystalline cellulose, povidone and sodium starch glycolate. For the latest FDA MedWatch alerts, Missing a dose of Acyclovir Tablets could cause a reactivation of a virus being treated. Search FDA . Recommended Mar 2012; Revised Feb 2019, Sept 2019 . Acyclovir Tablets, USP is a formulation for oral administration.Each Acyclovir Tablet contains 400 mg or 800 mg of acyclovir. ACYCLOVIR: 200MG/5ML: SUSPENSION;ORAL: Prescription: AB: Yes: Yes: Approval Date(s) and History, Letters, Labels, Reviews for NDA 019909. For the latest FDA MedWatch alerts, go here. Sustiva FDA Alerts. Available for Android and iOS devices. Serious adverse events reported in the clinical studies, for which a drug relationship could not be excluded, were atrial fibrillation, chest pain, diarrhea, digitalis intoxication, gastrointestinal hemorrhage, hyperglycemia, hyperuricemia, hypokalemia, hypotension, hypovolemia, shunt thrombosis, rash, rectal bleeding, syncope, and ventricular tachycardia.The affected lot of Acyclovir 400mg Tablet is Lot 19900 with an expiration date of 05/2019. : 20-972 Approval Date: 9/17/1998 . Following is a list of possible medication recalls, market withdrawals, alerts and warnings. The FDA Alert(s) below may be specifically about acyclovir or relate to a group or class of drugs which include acyclovir.MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. The FDA Alert(s) below may be specifically about acyclovir or relate to a group or class of drugs which include acyclovir. MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com.

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