Perrigo Company announced that it has initiated a voluntary product recall in the US to the retail level of 2 batches of its children's cough medicine.
Cough Syrup Overdose Puts 14-Year-Old in Acute Confusional State
Excessive consumption of over-the-counter cough syrup containing codeine has led to confusional state in a healthy 14-year-old girl.
Excessive consumption of over-the-counter cough syrup containing codeine has led to confusional state in a healthy 14-year-old girl.
‘Two types of children's cough syrup are being recalled by Perigo Company in US after dosing cups with incorrect markings were included in the packaging, prompting concerns of an accidental overdose.’
The company has asked people to throw away the dosage cup as it could potentially lead to overdose. The medications are sold at nine major stores under different brand names like CVS, Dollar General and Rite Aid across the country and the US Food and Drug Administration (FDA) is aware of the recall. Perrigo's Chairman and CEO Joseph C. Papa said, "There have been no reports of adverse events to Perrigo as a result of the incorrect dosage markings. Perrigo is taking this action to maintain the highest possible product quality standards for our retail customers and consumers. We are taking this action because it is the right thing to do."
The company also warned parents about the possible side effects of an overdose of Guaifenesin DM. It includes hyperexcitability, rapid eye movements, changes in muscle reflexes, ataxia, dystonia, hallucinations, stupor and coma. Other effects have included nausea, vomiting, tachycardia, irregular heartbeat, seizures, respiratory depression, and death.
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The Centers for Disease Control and Prevention (CDC) data shows there were 47,055 deaths from drug overdose across the country in 2014.
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Dr Reddy's Laboratories is recalling Amlodipine besylate and Atorvastatin calcium tablets in strengths including 2.5mg/10mg, 2.5 mg/20mg and 10mg /80mg.
Dr Reddy's Laboratories is recalling Amlodipine besylate and Atorvastatin calcium tablets in strengths including 2.5mg/10mg, 2.5 mg/20mg and 10mg /80mg.
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The drug firm voluntarily recalled the devices after dose-dispensing problems were identified in internal quality reviews and after 26 reports from consumers.
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