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

DEATH ( 55 FDA reports)
FALL ( 14 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
MUSCLE RIGIDITY ( 10 FDA reports)
HALLUCINATION ( 9 FDA reports)
HYPERKINESIA ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
PARKINSON'S DISEASE ( 7 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
NODULE ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INJECTION SITE INFLAMMATION ( 5 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
DEVICE MALFUNCTION ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INFUSION SITE MASS ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
PAIN ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFUSION SITE ABSCESS ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEVICE COLOUR ISSUE ( 1 FDA reports)
DEVICE COMPUTER ISSUE ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INDURATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MULTIMORBIDITY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ON AND OFF PHENOMENON ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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