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

DEMYELINATION ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
PAIN ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
APHASIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
ASTHMA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
FALL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STRESS ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GOUT ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)