Comtess and blood creatinine increased Patient Reports February 11, 2012

Comtess Side Effects Report #4915192-5
Comtess side effect was reported by a Physician from FINLAND on Jan 19, 2006. Male patient, 79 years of age, was diagnosed with parkinson's disease  and was treated with Comtess. After drug was administered, patient experienced the following side effects: arthralgia, blood creatinine increased, blood urea increased, c-reactive protein increased, dizziness , nausea , rash , swelling. Comtess dosage: unknown. During the same period patient was treated with SINEMET CR, WARFARIN, LOSARTAN POTASSIUM, ROPINIROLE. Patient was hospitalized. Patient recovered.

Comtess Side Effects Report #4931397-1
Comtess side effect was reported by a Physician from FINLAND on Jan 19, 2006. Male patient, 79 years of age, was diagnosed with parkinson's disease  and was treated with Comtess. After drug was administered, patient experienced the following side effects: arthralgia, blood creatinine increased, blood urea increased, c-reactive protein increased, dizziness , nausea , rash , swelling. Comtess dosage: unknown. During the same period patient was treated with SINEMET CR, WARFARIN, LOSARTAN POTASSIUM, ROPINIROLE. Patient was hospitalized. Patient recovered.

Comtess Side Effects Report #4919670-4
Comtess side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 27, 2006. Male patient, 70 years of age, was diagnosed with parkinson's disease  and was treated with Comtess. After drug was administered, patient experienced the following side effects: arthralgia, blood creatinine increased, blood urea increased, dizziness , joint swelling, nausea , oedema peripheral, pain in extremity, rash . Comtess dosage: 600 MG (200 MG, 3 IN 1 D), ORAL. During the same period patient was treated with SINEMET CR, WARFARIN, LOSARTAN POTASSIUM, ROPINIROLE, FRUSEMIDE. Patient was hospitalized. Patient recovered.