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

HERPES ZOSTER ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
COMA ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
FALL ( 3 FDA reports)
FEMORAL NECK FRACTURE ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
RENAL CANCER METASTATIC ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

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