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Huliq News Tagged: "US FDA"

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FDA Approves New Drug to Treat Rare Disease, Acromegaly

The U.S. Food and Drug Administration today (August 30) approved Somatuline Depot (lanreotide acetate injection) for the treatment of acromegaly, a rare and potentially life threatening disease in adults caused by abnormal secretion of growth hormone (GH), commonly from a benign tumor located in the pituitary gland located in the brain.

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FDA Approves Human Thrombin for Topical Use in Surgery

The U.S. Food and Drug Administration approved Evithrom (human thrombin), a blood-clotting protein used to help control bleeding during surgery.

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FDA Approves Second West Nile Virus Screening Test for Donated Blood and Organs

The U.S. Food and Drug Administration today (August 28) announced approval of a second test for the detection of West Nile virus (WNV) in blood and organs.

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Mars Petcare US, Inc. Recalls Dry Dog Food

The U.S. Food and Drug Administration is alerting consumers that Mars Petcare US, Inc. has recalled two dry dog food products because of the potential contamination with Salmonella Schwarzengrund.

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FDA Expands Warning on Eating Raw Oysters

Additional Growing Area Linked to Illness Outbreaks

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FDA Proposes New Rule for Sunscreen Products

Highlights Include New UVA Rating System, Sun Warning Information

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FDA Approves Risperdal for Two Psychiatric Conditions in Children and Adolescents

The U.S. Food and Drug Administration today (August 22) approved Risperdal (risperidone) for the treatment of schizophrenia in adolescents, ages 13 to 17, and for the short-term treatment of manic or mixed episodes of bipolar I disorder in children and adolescents ages 10 to 17. This is the first FDA approval of an atypical antipsychotic drug to treat either disorder in these age groups.

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FDA Warning on Codeine Use by Nursing Mothers

May Increase Chance of Serious Side Effects in Infants

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Recall of Metaboslim Capsules Due to Potential Health Risks

Health Canada is advising Canadians of a recall in the United States of one lot of Metaboslim Apple Cider Vinegar, which is marketed as a dietary supplement, because it has been found to contain sibutramine, a prescription medication that should only be taken under medical supervision.

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FDA Approves Updated Warfarin (Coumadin) Prescribing Information

New Genetic Information May Help Providers Improve Initial Dosing Estimates of the Anticoagulant for Individual Patients

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Manufacturers of Diabetes Drugs to Strengthen Warning on Heart Failure Risk

The U.S. Food and Drug Administration today (August 14) announced manufacturers of certain drugs approved to treat Type 2 diabetes have agreed to add a stronger warning on the risk of heart failure, a condition that occurs when the heart does not adequately pump blood.

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New Approvals From FDA

FDA Grants Tentative Approval for 50th and 51st Anti-Retroviral Drugs Under President's AIDS Relief Plan

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