THEOLAIR Safety Questions, THEOLAIR Answers
More Here>>Side Effects - FDA Reports 2006-2008
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THEOLAIR Safety Reports
Total THEOLAIR reports: 1.THEOLAIR FDA safety alerts: No.
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Consumer or non-health professional from NETHERLANDS reported THEOLAIR problem on Sept 07, 2006. Male patient, 59 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with THEOLAIR. After drug was administered, patient experienced the following problems/side effects: cold sweat, fatigue, muscle contractions involuntary, myalgia, oedema, osteoporosis, palpitations, tachycardia. THEOLAIR dosage: 700 MG (350 MG, 2 IN 1 DAY (S)) ORAL. During the same period patient was treated with SERETIDE. Patient recovered.