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Page 10 - Adverse Event Reporting Program News Today : Breaking News, Live Updates & Top Stories | Vimarsana

Cordis US Corp Recalls INFINITI Angiographic Catheter due to Products Being Shipped Without Undergoing Sterilization Procedures

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death

Adverse event reporting programDrug administrationCordis us corpUrgent medical device recall noticeUrgent medical device recallAcknowledgement formCordis customer support

FDA Warns Against Neptune s Fix Because of Serious Health Risks

The FDA is warning consumers not to use Neptune's Fix or other tianeptine products because of seiorus health risks, including seizures.

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Fatal Reaction Risks On Certain Seizure Medications: A FDA Warning

FDA alerts on seizure meds' fatal reactions. Stay informed about the risks and safeguard yourself. Read more.

United statesDrug administrationAdverse event reporting programEvent reporting systemVeterinarians warn petWatch safety information

Gas Station Heroin Supplement Causes Seizures, Loss Of Consciousness, FDA Warns

Neptune s Fix, a product sold illegally with claims to improve brain function and treat conditions such as anxiety, depression, pain and opioid use disorder, contains a potentially dangerous

Poison control centerAdverse event reporting programDrug administrationWatch safety informationUs worldNeptunes fixGas station heroinLoss of consciousnessFda warns

Bayer Recalls Oral Larotrectinib Solution Because of Microbial Contamination

OncLive serves as the connection to oncology, including groundbreaking cancer news and interviews with top oncologists in multimedia formats.

National drug codeAdverse event reporting programBayer medical information call centerUnited statessWatch safety informationPrecision medicine

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