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

ARTHROPATHY ( 5 FDA reports)
MALAISE ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
FALL ( 4 FDA reports)
AGITATION ( 3 FDA reports)
RASH ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PAIN ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
VASCULITIS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
HEPATIC ENZYME DECREASED ( 1 FDA reports)
COUGH ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
COMA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ABASIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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