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

RENAL FAILURE ACUTE ( 15 FDA reports)
HYPONATRAEMIA ( 12 FDA reports)
ASTHENIA ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
FALL ( 9 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
VERTIGO ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
METASTASES TO LIVER ( 6 FDA reports)
RECTOSIGMOID CANCER ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
VOMITING ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
COMA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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