Please choose an event type to view the corresponding MedsFacts report:

DRUG INEFFECTIVE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PAIN ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PENIS CARCINOMA STAGE IV ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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