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

ABDOMINAL DISCOMFORT ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
SCAR ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARBUNCLE ( 2 FDA reports)
RASH ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
CORONARY ARTERY EMBOLISM ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
APHONIA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
CRYING ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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