Watson Announces Limited Recall Of Fentanyl Transdermal System

... this product, and/or quality problems should also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the medwatch Web site at www.fda.gov/medwatch . Watson's Fentanyl Transdermal Sy...

CCHRINT Announces FDA Reported Psychiatric Drug Side Effects Search Engine

...s and consumers have been decrypted from the FDA's medwatch reporting system and been made available to the pu...ort totals reveal that between 2004-2008 the FDA's medwatch system received pregnancy-related psychiatric drug... between 2004-2008 there were reports submitted to medwatch including 4,895 suicides, 3,908 cases of aggressio...

INVEGA(R) Approved as the First and Only Treatment for Schizoaffective Disorder

...erapy, talk with your doctor. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.g o v / medwatch , or call 1-800-FDA-1088. About INVEGA(R) INVEGA(R), an atypical antipsychotic medication, was first approved in the U.S. in December 2006...

CareFusion Issues Update Regarding Previously Disclosed June 12, 2009 Recall of the Alaris(R) System

...ed of this action. Any adverse reactions experienced with the use of this product, and/or quality problems should also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA 5600 Fishers Lane, Rockville, MD 20852-9787, or at www....

FDA Tells Patients to Stick With Diabetes Drug Linked to Cancer

...meantime, the FDA says it "encourages both health care professionals and patients to report side effects from the use of insulin glargine to the FDA's medwatch Adverse Event Reporting Program." More information Find out more about diabetes at the American Diabetes Association . ...

Biosite Incorporated Issues Voluntary, Nationwide Recall for Cardiac Marker Test

... of this product, and/or quality problems can also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the medwatch website at www.fda.gov/medwatch . ...

Caraco Pharmaceutical Laboratories, Ltd. Announces a Nationwide Voluntary Recall of All Lots of Digoxin Tablets Due to Size Variability

...ected product, and/or quality problems should also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at Med Watch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the medwatch website at www.fda.gov/medwatch . Detroit-based Caraco Pharmaceutical...

Sparta Systems to Address Critical Electronic Medical Device Reporting (eMDR) Concerns with Free Webinar

...ebinar scheduled to "go live" on Tuesday, Feb. 10, 2009 at 2:00 p.m. EST. Due to the overwhelming volume of paper-based medwatch 3500A reports received by the FDA's Center for Devices and Radiological Health (CDRH) in recent years, the agency has ...

Ther-Rx Corporation Issues Voluntary Nationwide Recall of Prescription Prenatal and Iron Supplements to Wholesale Level

...rienced with the use of these products should also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the medwatch website at www.fda.gov/medwatch . The recall announcement is posted o...

ETHEX Corporation Issues Voluntary Nationwide Recall of Prescription Prenatal and Iron Supplements to Wholesale Level

...experienced with the use of these products should also be reported to FDA's medwatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the medwatch website at www.fda.gov/medwatch . The recall announcement is posted o...

MedWatch in Medical Technology

FDA MedWatch: Avastin (bevacizumab) and Formation of Tracheoesophageal Fistula in a Recent Clinical Study in Patients with Limited-stage Small Cell Lung Cancer

...ackage insert to include more detailed information regarding the incidence of all cases of fistula in patients treated with Avastin. Read the complete medwatch 2007 Safety Alert with links to the Genentech Dear Healthcare Professional Letter and the most recent Avastin labeling, at:

ETHEX Corporation Issues Nationwide Voluntary Recall of Products

...rienced with the use of these products should also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the medwatch website at http://www.fda.gov/medwatch . The recall announcement is...

Ther-Rx Corporation Issues Nationwide Voluntary Recall of Products

...rienced with the use of these products should also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the medwatch website at http://www.fda.gov/medwatch . The recall announcement is...

ETHEX Corporation Voluntarily Recalls Specific Lots of 30 mg. and 60 mg. Morphine Sulfate Extended Release Tablets Due to the Potential for Oversized Tablets

...Drug Administration (FDA). Any adverse reactions experienced with the use of this product, and/or quality problems may also be reported to the FDA's medwatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatc...

iGuard Transforms Drug Safety Alert and Update Process

...Patients are instructed to give the form to their physician for completion. medwatch is the U.S. Food and Drug Administration's safety information and adverse e...ed submit the forms to the FDA. Because the data are ultimately reported to medwatch by the patient's physician, iGuard is a patient-driven, physician-reported ...