Comtess and nausea 
Comtess and nausea Patient Reports February 11, 2012
Comtess Side Effects Report #4564573-0
Comtess side effect was reported by a Consumer or non-health professional from on Mar 05, 2002. Female patient, 68 years of age, was diagnosed with parkinsonism and was treated with Comtess. After drug was administered, patient experienced the following side effects: abdominal adhesions, cardiac arrest
, cardiac failure, gastric perforation, gastrointestinal necrosis, ileus, intestinal gangrene, nausea , pallor. Comtess dosage: 200 MG ORAL. During the same period patient was treated with FLUNITRAZEPAM, SINEMET DEPOT, MADOPARK, BEHEPAN, REMERON. Patient was hospitalized. Patient recovered.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.