A brief guide to Avandamet recalls
The prescription medication Avandamet is prescribed to both those at risk for type II diabetes as well as those trying to control the effects of this condition. An Avandamet recall is unlikely to occur during a course of treatment. While taking this medication, you should be aware of the many potential side effects that may occur. However, Avandamet recalls due to inadequately manufactured medication are unlikely to interrupt your course of treatment.
There are two active ingredients in this medication, metformin and rosiglitazone. In 2010, there was an Avandamet recall issued by the FDA because the amount of the latter drug was incorrect in some medication. This medication's effectiveness varies from patient to patient based on small adjustments of the dosage. Avandamet recalls were deemed necessary because issuing medication with the incorrect amount of one of the active ingredients undermined physicians' ability to supervise patient treatment, as well as the health of the patient.
An Avandamet recall is an unusual event which is unlikely to recur. Many safety issues have been raised concerning side effects initially not warned against in the medication's packaging. However, Avandamet recalls do not occur solely because of some reports of serious side effects. The manufacturer's information on the drug has been updated to note these potential side effects.
Reports that the drug led to an increased risk of side effects did not result in an Avandamet recall. Additionally, usage of the drug has been associated with an increasing risk of bond damage and breaking. While FDA warnings have been issued summarizing these incidents, they did not lead to Avandamet recalls.
Before issuing this drug, a physician should explain all of these possible risks which must be monitored for. While you should not worry about having your treatment interrupted by an Avandamet recall, this is unlikely to be the case. However, a physician may discontinue use if you report any allergic responses to ingestion, such as swelling in your tongue or throat. While they report unexpected adverse effects to the FDA, this will not automatically lead to Avandamet recalls.
Report any repeating side effects to a physician. You should not wait for an Avandamet recall if you think usage should be discontinued. However, do not cease intake until you have consulted with your physician. If Avandamet recalls occur, consult with your physician immediately.
If you consume medication before it has been warned against in an Avandamet recall, you may have grounds for litigation. In the unlikely event that Avandamet recalls concern your prescription medication, consult with a lawyer as soon as possible to discuss the viability of litigation. A lawsuit can be filed on behalf of one person or as a class-action suit on behalf of many different individuals who have suffered the same adverse effects. To ensure you do not take action after your state's statute of limitations has expired, speak with an attorney as soon as possible. Maintain copies relating to the purchase of all medication if you must prove that your tablets were among those cited in an Avandamet recall.
