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HAEMOLYTIC ANAEMIA ( 5 FDA reports)
FALL ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DERMATITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TREMOR ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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