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BACK PAIN ( 4 FDA reports)
FATIGUE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
FALL ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)

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