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

HYPONATRAEMIA ( 12 FDA reports)
ASTHENIA ( 10 FDA reports)
FALL ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
MYALGIA ( 7 FDA reports)
VASCULAR PURPURA ( 7 FDA reports)
DIZZINESS ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
INFECTION ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
OSTEONECROSIS OF JAW ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COUGH ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSLOGIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LYMPHOCELE ( 4 FDA reports)
MALAISE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COMA ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GRIP STRENGTH ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
MASS ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLATELET AGGREGATION INCREASED ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UNDERDOSE ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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