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GlossaryMedWatch

program for reporting adverse drug and device events

MedWatch is the FDA's safety information and adverse event reporting program. It allows healthcare professionals and consumers to report serious problems they suspect are associated with the drugs and medical devices they prescribe, dispense, or use. This helps the FDA monitor product safety and take necessary actions to protect public health.

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research Hyperammonemia with Valproic Acid: Colonic Ischemia Associated with Triptan Use, Visual Side Effects with Pegylated Interferon, Alopecia Areata with Infliximab, and Adverse Effects Seen with Medications Used for Irritable Bowel Syndrome

2 citations, November 2004 in “Hospital pharmacy”

Certain medications can cause serious side effects, so it's important to report them.

research Acute Encephalomyelitis Syndromes Associated with H1N1 Influenza Vaccinations; Erythema Multiforme Secondary to H1N1 Vaccine; Cytolytic Hepatitis Possibly Related to Oral Contraceptives; Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) Syndrome Associated with Lamotrigine: First Report; Behavioral Disinhibition with Baclofen; Minoxidil-Induced Trichostasis Spinulosa of Terminal Hair; Delayed-Onset Mirtazapine-Related Leukopenia

1 citations, March 2011 in “Hospital Pharmacy”

Various medications and vaccines can cause serious side effects.

research Cerebral Ischemia Related to Isotretinoin; Venlafaxine-Induced Alopecia; Cognitive Dysfunction with Tolterodine; Retinal Artery Occlusion After Injection of Long-Acting Risperidone; Olanzapine-Induced Chylomicronemia Presenting as Pancreatitis; Metabolic Effects of the Atypical Antipsychotics – An Editorial; Another Drug-Induced Pancreatitis – This One Caused by a Tyrosine Kinase Inhibitor; Suicide Attempts Related to Antidepressant Medications

November 2007 in “Hospital pharmacy”

The conclusion is that healthcare professionals should report adverse drug reactions to improve medication safety and patient care.

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