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

DIARRHOEA ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
CORONARY ARTERY THROMBOSIS ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
FALL ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SCIATICA ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FIBROMYALGIA ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PAIN ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
TONGUE DRY ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CYST ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYELOMA RECURRENCE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ORAL CAVITY FISTULA ( 1 FDA reports)
OROANTRAL FISTULA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALATAL DISORDER ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURPURA SENILE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLIPPING RIB SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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