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

VISUAL FIELD DEFECT ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FALL ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)

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