Church & Dwight Co., Inc. has issued a recall of several Zicam and Orajel products due to microbial contamination.

Church & Dwight Co., Inc. is voluntarily recalling all lots within expiry of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal ...

The National Agency for Food and Drug Administration and Control has urged Nigerians and healthcare practitioners to report any unusual ... just about medicines. Adverse events following ...

ISLAMABAD: The Drug Regulatory Authority of Pakistan (DRAP) as a part of continued crackdown against falsified/spurious drugs has issued an immediate recall alert for Gabica Capsule 300 mg, which ...

1 Division of General Medical Sciences, John T Milliken Department of Medicine, Washington University School of Medicine in St Louis, St Louis, MO, USA 2 Center for Advancing Health Services, Policy ...

Since the MMR vaccine was released in 1971, there have been more than 103,000 adverse reaction reports submitted to the CDC's Vaccine Adverse Event Reporting ... for various forms of DTaP, the ...

The form also asks whether the person has a ... Data in the Vaccine Adverse Event Reporting System can be submitted by anyone, and the CDC warns in several places that it cannot be used to ...

“The content of this draft reporting form is not final and the text may be subjected ... called for timely reporting of adverse events related to medical devices. The recent draft format for IVD, ...

The drugs had the same active ingredients, the same dosage form and the same ... the United States. These adverse event reports are available in the FDA Adverse Event Reporting System (FAERS).

Such equipment form a critical part in medical diagnosis ... with no comprehensive system for adverse event reporting. There’s a need to align with international standards and enhance safety ...