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

PAIN ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
STATUS EPILEPTICUS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
VOMITING ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DIZZINESS ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ABDOMINAL WALL INFECTION ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CRYING ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
FALL ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
DEATH ( 1 FDA reports)
ULCER ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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