Qualitest, a subsidiary of Endo Health Solutions, has issued a voluntary nationwide recall for 101 lots of Hydrocodone Bitartrate and Acetaminophen Tablets , USP 10 mg/500 mg. Bottles from the affected lots may contain tablets that have a higher dosage of acetaminophen, and as a result, it is possible that consumers could take more than the intended acetaminophen dose.
The problem with getting too much acetaminophen is that it could result in liver toxicity, especially in patients on other acetaminophen containing medications, patients with liver dysfunction, or people who consume more than three alcoholic beverages a day.
The affected lots, were distributed between Feb. 20, 2012 and Nov. 19, 2012 to wholesale distributors and retail pharmacies nationwide. For a list of the lot numbers, see Qualitest's press release .
If you have hydrocodone/acetaminophen tablets from the affected lots, contact Qualitest at 1-800-444-4011. If you are unsure if you have the affected ...
For some reason, Tramadol is an overlooked, misunderstood drug. Even some doctors are confused about some facts that seem to be little known. Most know that tramadol is used to treat pain and comes in both short acting and time released formulas. Various brand name drugs contain tramadol including: Ultracet, Ultram, Ultram ER, Ryzolt, and Rybix. Because these all contain tramadol, they are all worth considering even for the toughest to treat pain. But first, let's clear up some confusion about tramadol.
Is tramadol an opioid? So many people have been lead to believe that tramadol is not an opioid medication. In fact, tramadol is considered an opioid medication because it like morphine and hydrocodone bind to and activate the mu opioid receptor . This mechanism provides the pain relieving, the analgesic effect. And like all the other opioids, the regular use of tramadol can lead to physical dependency . Thus, when this exogenous source of opioids is withdrawn suddenly, a per...
The all-out effort to make all opioid pain-relieving medications more difficult to get continues. Last week an FDA panel voted 19 to 10 to reclassify medications that contain hydrocodone – like Vicodin and Lortab – from Schedule III drugs to Schedule II drugs.
Currently, under the federal Controlled Substances Act, medications containing hydrocodone are classified as Schedule III drugs. This means doctors can call in or fax prescriptions to the pharmacy and can allow up to five refills in a six-month period.
If hydrocodone-containing products are reclassified to Schedule II, only written prescriptions with an original signature by the physician are acceptable and no refills are allowed. If you take a hydrocodone medication on a regular basis, that means in most cases you'll have to go to your doctor's office every month to get a new prescription.
The DEA (Drug Enforcement Administration) does allow, but does not encourage, doctors to issue multiple pre...
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