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

HALLUCINATION ( 7 FDA reports)
ABSCESS ( 6 FDA reports)
INFUSION SITE ERYTHEMA ( 6 FDA reports)
PSYCHOTIC DISORDER ( 6 FDA reports)
FALL ( 5 FDA reports)
INFUSION SITE MASS ( 5 FDA reports)
TREMOR ( 5 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
NODULE ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
INFUSION SITE NECROSIS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFUSION SITE ABSCESS ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE INDURATION ( 2 FDA reports)
INFUSION SITE WARMTH ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTED EPIDERMAL CYST ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SEXUAL OFFENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)

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