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Ibuprofen and Oxcarbazepine Tablets Recalled: AttorneyOne Monitors and Keep Consumers Informed
Date:7/25/2014

San Diego, CA (PRWEB) July 25, 2014

AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Ibuprofen and Oxcarbazepine Tablets.

The FDA published on July 21, that one lot of Ibuprofen and one lot of Oxcarbazepine Tablets, by American Health Packaging (AHP), are recalled due to mislabeled packaging. Oxcarbazepine is used for the treatment of certain types of seizures in patients with epilepsy.

The reason for the recall is that Lot #142588, Expiration Date, 01/2016 of Ibuprofen Tablets, USP, 600 mg, in a hospital unit dose presentation may contain individual blistered doses labeled as Oxcarbazepine Tablets, 300 mg, lot #142544. Lot #142544 of Oxcarbazepine Tablets, 300 mg, is also recalled. This mislabeling can cause patients receiving ibuprofen and missing their scheduled dose of oxcarbazepine; this may lead to increased chances of having a seizure. Moreover, if ibuprofen is taken in cases where it is contraindicated it may cause adverse reactions.

Taking into consideration the latest developments, AttorneyOne.com monitor daily and update the website providing accurate information on all relevant FDA safety alerts. Sean Burke, director of Media Relations at AttorneyOne.com, adds, “We are determined to keep an eye on FDA announcements concerning Ibuprofen and Oxcarbazepine Table
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