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

ABDOMINAL DISCOMFORT ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
COLONIC HAEMATOMA ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
AGGRESSION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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