Comtess Safety Reports submitted to FDA
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More Rx Information: A B C D E F G H I J K L M N O P Q R S T U V W X Y ZTotal Comtess reports: 11.
Comtess FDA safety alerts: No.
Reported hospitalizations: 7.
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FDA Reported Comtess Side Effects: rectal haemorrhage, international normalised ratio increased, contusion, chest pain, confusional state, tooth loss, prostate cancer, clostridium difficile toxin test positive, bedridden, bacteria urine identified, atrophy.
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Comtess Side Effects Report #5216559-0
Health Professional from UNITED KINGDOM reported COMTESS problem on Jan 02, 2007. Male patient, 52 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: pneumonia. COMTESS dosage: unknown. During the same period patient was treated with TEGRETOL, LIPRINEL CAP. Patient was hospitalized. Patient recovered.
Comtess Side Effects Report #5259333-1
COMTESS problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Feb 13, 2007. Male patient, 72 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: asthenia, hypokinesia, mobility decreased, on and off phenomenon. COMTESS dosage: unknown. During the same period patient was treated with ROPINIROLE, AMANTADINE, DUTASTERIDE, TAMSULOSIN, LANSOPRAZOLE, MOVICOL, REGULAN. Patient recovered.
Comtess Side Effects Report #5057066-8
Health Professional from DENMARK reported COMTESS problem on July 05, 2006. Male patient, 74 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, blood alkaline phosphatase increased, blood amylase decreased, blood amylase increased, chromaturia, confusional state, coombs direct test positive, fatigue, flatulence. COMTESS dosage: 1400 MG ORAL. During the same period patient was treated with MADOPAR, APOMORFIN, AMANTADINE, SIFROL, SEROQUEL, DETRUSITOL, ARICEPT, MOTILIUM. Patient recovered.
Comtess Side Effects Report #5075751-9
COMTESS problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 26, 2006. Male patient, 84 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: contusion, international normalised ratio increased, rectal haemorrhage. COMTESS dosage: unknown. During the same period patient was treated with WARFARIN, MADOPAR, QUININE SULPHATE, RAMIPRIL, FALODIPINE MR, AMIODARONE HYDROCHLORIDE. Patient was hospitalized and became disabled. Patient recovered.
Comtess Side Effects Report #5075754-4
Consumer or non-health professional from SWEDEN reported COMTESS problem on July 26, 2006. Female patient, 76 years of age, was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: bradycardia, cardiac arrest. COMTESS dosage: unknown. During the same period patient was treated with ROBINUL, SINEMET DEPOT, METFORMIN, TIENAM. Patient recovered.
Comtess Side Effects Report #5089426-3
COMTESS problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Aug 03, 2006. Male patient was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: chest pain. COMTESS dosage: unknown. Patient was hospitalized. Patient recovered.
Comtess Side Effects Report #5097622-4
Consumer or non-health professional from UNITED KINGDOM reported COMTESS problem on Aug 03, 2006. Male patient, 84 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: contusion, international normalised ratio increased, rectal haemorrhage. COMTESS dosage: 200 MG; 400 MG (200 MG, 2 IN 1 D) ; 600 MG (200 MG, 3 IN 1 D). During the same period patient was treated with MADOPAR, QUININE SULPHATE, RAMIPRIL, FALODIPINE MR, AMIODARONE HYDROCHLORIDE, FUROSEMIDE. Patient was hospitalized and became disabled. Patient recovered.
Comtess Side Effects Report #5109700-1
COMTESS problem was reported by a Physician from UNITED KINGDOM on Sept 11, 2006. Male patient, 84 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: confusional state, contusion, international normalised ratio increased, rectal haemorrhage, refusal of treatment by relative. COMTESS dosage: unknown. During the same period patient was treated with WARFARIN, MADOPAR, QUININE SULPHATE, RAMIPRIL, FELODIPINE, AMIODARONE, FUROSEMIDE. Patient was hospitalized and became disabled. Patient recovered.
Comtess Side Effects Report #5129954-5
Consumer or non-health professional from GERMANY reported COMTESS problem on Sept 29, 2006. Male patient, 75 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: renal failure, rhabdomyolysis. COMTESS dosage: unknown. Patient was hospitalized. Patient recovered.
Comtess Side Effects Report #5154546-1
COMTESS problem was reported by a Consumer or non-health professional from FINLAND on Oct 23, 2006. Female patient, 76 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: aggression, anorexia, antigliadin antibody positive, asthma, atrophy, bacteria urine identified, bedridden, chest pain, clostridium difficile toxin test positive. COMTESS dosage: 1200 + 600 MG (200 MG, 6 IN 1 D). During the same period patient was treated with KARDOPAL, SINEMET DEPOT, ATACAND, THYROXIN, PULMICORT, SEREVENT, IMDUR DEPOT. Patient was hospitalized. Patient recovered.
Comtess Side Effects Report #5194515-9
Consumer or non-health professional from UNITED KINGDOM reported COMTESS problem on Dec 04, 2006. Male patient, 65 years of age, was diagnosed with parkinson's disease and was treated with COMTESS. After drug was administered, patient experienced the following problems/side effects: prostate cancer, tooth loss. COMTESS dosage: 800 MG (200 MG, 4 IN 1 D) ORAL. During the same period patient was treated with SINEMET, SELEGILINE, ROPINROLE. Patient recovered.
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