Actos
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Actos
OVERDOSE
During controlled clinical trials, one case of overdose with ACTOS was reported. A male patient took 120 mg per day for four days, then 180 mg per day for seven days. The patient denied any clinical symptoms during this period.
In the event of overdosage, appropriate supportive treatment should be initiated according to the patient's clinical signs and symptoms.
CONTRAINDICATIONS
Do not initiate in patients with NYHA Class III or IV heart failure [see BOXED WARNING].
Do not use in patients with a history of a serious hypersensitivity reaction to ACTOS or any of its ingredients.
Last reviewed on RxList: 8/10/2011
This monograph has been modified to include the generic and brand name in many instances.
Additional Actos Information
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