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Recent Posts
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- FDA Safety Warning For Multaq, A Heart Rhythm Drug
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- Physical Therapy Not Only for Rehabilitation
- Bears’ Receiver Faces 4 Months of Recovery
- About 21,600 Honda Goldwing Motorcycles Recalled
- DUI Suspect Collides Head-On With Vehicle
- Fatal Highway 101 Crash Leaves One Dead, One Injured
Tag Archives: adverse-effects
FDA Safety Warning For Multaq, A Heart Rhythm Drug
According to news sources , the drug Multaq is getting a new safety warning after a study found increased risks of heart attack, stroke and death associated with the drug with a subset of patients that took part in the study. The heart rhythm drug controls the heart’s chambers by allowing them to pump in sync for patients with atrial fibrillation. The new warning would allow the drug to remain on the market but would stress to doctors and patients that it be used only for treatment of the short-term variant of the condition Continue reading
Nasal Spray Recalled for Bacteria
34,092 Nostrilla bottles have been recalled due to the spray potentially containing bacteria. The spray is used as a nasal decongestant to relieve nasal discomfort during colds. Continue reading
Nostrilla Recalled for Bacteria Contamination
34,092 bottles of Nostrilla are undergoing a recall due to the finding that the spray may contain bacteria. The recalled spray is used as a nasal decongestant for the relief of nasal discomfort during colds. Continue reading
Posted in Car Accident, Personal Injury, personal injury lawyer, Product Liability, Product Recall, Safety, Uncategorized
Tagged adverse-effects, car accident lawyer, country, expiration-date, nasal spray safety, personal injury lawyer, personal-injury, plastic-bottle, product, product liability, recalled nasal spray, safety, weakened-immune
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Povidone Iodine Recalled Due to Lack of Inspection
In a press release , H&P Industries Inc, a manufacturer of over-the-counter drug products, announced the voluntary recall of all lots of Povidone Iodine Swabsticks, Prep Solutions, Scrub Solutions and Prep Gels in cooperation with the US Food and Drug Administration (FDA) due to the lack of oversight infrastructure at the time of production. The recall of these Povidone Iodine products is being initiated because H&P Industries produced them without having a system in place for microbial testing at the time of release, having a system in place to test incoming components and without having procedures set and in place to prevent objectionable microorganisms in these products. The company has conducted an extensive investigation and testing and has not found any evidence of contamination Continue reading