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

PAIN ( 7 FDA reports)
PRURITUS ( 5 FDA reports)
FALL ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
MALAISE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
COUGH ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJURY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEAR ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DEATH ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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