1-100 of about 215 matches for site:www.fda.gov food regimen
The Food and Drug Administration approved revisions to the TRIUMEQ (abacavir/dolutegravir/lamivudine
https://www.fda.gov/drugs/human-immunodeficiency-virus-hiv/food-and-dr...
The Food and Drug Administration approved revisions to the TRIUMEQ (abacavir/dolutegravir/lamivudine
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of Approved Medically Important Antimicrobial Drugs Administered in the Feed of Food-Producing Animals that Lack
FDA approves treosulfan with fludarabine as a preparative regimen for alloHSCT in adult and pediatri
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FDA approves treosulfan with fludarabine as a preparative regimen for alloHSCT in adult and
FDA Announces Plan to Phase Out Animal Testing Requirement for Monoclonal Antibodies and Other Drugs
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Information about Mifepristone for Medical Termination of Pregnancy Through Ten Weeks Gestation | FD
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interstate commerce until a food additive regulation is promulgated by the U.S. Food and Drug
Complementary and Alternative Medicine Products and their Regulation by the Food and Drug Administra
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Food Additive Safety (HFS-200), Center for Food Safety and Applied Nutrition, Food And Drug
https://www.fda.gov/drugs/hiv-treatment/hiv-treatment-information-adul...
and ritonavir 20 mg/mL Combination Products Oral Solution Given once daily or twice daily regimen with food. Please see
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surface area. Must be given with food. Please see Full Prescribing Information for dosing regimen. Kaletra Label Odefsey* emtricitabine
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withdrawal time for the dosage regimen you are using. The dosage regimen includes: How much of
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Withdrawals and Safety Alerts Press Announcements Warning Letters Advisory Committees En Español Products Food Drugs Medical Devices Radiation
FDA approves addition of survival data to gilteritinib label for refractory AML with a FLT3 mutation
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https://www.fda.gov/animal-veterinary/antimicrobial-resistance/extrala...
website and that any information you provide is encrypted and transmitted securely. U.S. Food and Drug
Strategic Partnership Program Agroterrorism (SPPA) Initiative: Second Year Status Report July 2006 -
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Patients Industry Health Professionals Federal, State and Local Officials In this section : Food Defense Initiatives Food Defense
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FDA grants accelerated approval to zanubrutinib for relapsed or refractory follicular lymphoma | FDA
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FDA grants accelerated approval to umbralisib for marginal zone lymphoma and follicular lymphoma | F
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Questions and Answers on Mifepristone for Medical Termination of Pregnancy Through Ten Weeks Gestati
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FDA Drug Safety Communication: Safety Review update of Abacavir and possible increased risk of heart
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non-abacavir regimen. No statistically significant association between MI and the abacavir-containing regimen was detected (Mantel-Haenszel
Information about Mifepristone for Medical Termination of Pregnancy Through Ten Weeks Gestation | FD
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FDA grants accelerated approval to ponatinib with chemotherapy for newly diagnosed Philadelphia chro
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Setting Endotoxin Limits During Development of Investigational Oncology Drugs and Biological Product
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FDA Announces Plan to Phase Out Animal Testing Requirement for Monoclonal Antibodies and Other Drugs
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FDA grants accelerated approval to tisotumab vedotin-tftv for recurrent or metastatic cervical cance
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https://www.fda.gov/drugs/resources-information-approved-drugs/fda-gra...
website and that any information you provide is encrypted and transmitted securely. U.S. Food and Drug
https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-pro...
website and that any information you provide is encrypted and transmitted securely. U.S. Food and Drug
https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-pro...
website and that any information you provide is encrypted and transmitted securely. U.S. Food and Drug
https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-pro...
website and that any information you provide is encrypted and transmitted securely. U.S. Food and Drug
https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-pro...
website and that any information you provide is encrypted and transmitted securely. U.S. Food and Drug
https://www.fda.gov/vaccines-blood-biologics/cellular-gene-therapy-pro...
website and that any information you provide is encrypted and transmitted securely. U.S. Food and Drug
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https://www.fda.gov/drugs/drug-approvals-and-databases/drug-trials-sna...
background regimen. Subjects in Group 2 initiated SUNLENCA and an optimized background regimen on Day 1. The
https://www.fda.gov/vaccines-blood-biologics/approved-blood-products/c...
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FDA adds Boxed Warning to highlight correct dosing of Ocaliva (obeticholic acid) for patients with a
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Influenza A (H5N1) Virus Monovalent Vaccine, Adjuvanted, manufactured by ID Biomedical Corporation -
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FDA Drug Safety Communication: New information regarding QT prolongation with ondansetron (Zofran) |
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https://www.fda.gov/drugs/news-events-human-drugs/fda-approves-new-use...
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FDA Office of Clinical Pharmacology and International Society of Pharmacometrics (ISoP) Public Works
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https://www.fda.gov/animal-veterinary/unapproved-animal-drugs/generic-...
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FDA D.I.S.C.O. Burst Edition: FDA approval of Polivy (polatuzumab vedotin-piiq) for previously untre
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https://www.fda.gov/drugs/spotlight-cder-science/translating-in-vitro-...
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https://www.fda.gov/industry/designating-orphan-product-drugs-and-biol...
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https://www.fda.gov/drugs/news-events-human-drugs/fda-approves-first-o...
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https://www.fda.gov/animal-veterinary/product-safety-information/cattl...
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https://www.fda.gov/drugs/pre-ind-consultation-program/division-anti-v...
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FDA Rationale for Recognition Decision: Amoxicillin and Clavulanate against Haemophilus influenzae |
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WITHDRAWN: FDA grants accelerated approval to melphalan flufenamide for relapsed or refractory multi
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Amneal Pharmaceuticals, LLC. Issues a Nationwide Voluntary Recall of Vancomycin Hydrochloride for Or
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https://www.fda.gov/news-events/fda-voices/pepfar-fda-approves-200th-h...
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FDA identifies harm reported from sudden discontinuation of opioid pain medicines and requires label
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A Microgram of Prevention is Worth a Milligram of Cure: Preventing Medication Errors in Animals | FD
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FDA approves updated drug labeling including new indications and dosing regimens for capecitabine ta
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FDA identifies harm reported from sudden discontinuation of opioid pain medicines and requires label
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