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

DIARRHOEA ( 20 FDA reports)
DYSPNOEA ( 20 FDA reports)
ASTHENIA ( 19 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 19 FDA reports)
PARAESTHESIA ( 19 FDA reports)
PAIN ( 18 FDA reports)
ANXIETY ( 17 FDA reports)
COMPLETED SUICIDE ( 17 FDA reports)
FATIGUE ( 17 FDA reports)
INSOMNIA ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
ARTERIOSCLEROSIS ( 16 FDA reports)
BONE DISORDER ( 16 FDA reports)
BRONCHITIS ( 16 FDA reports)
CARDIAC VALVE ABSCESS ( 16 FDA reports)
COLITIS ISCHAEMIC ( 16 FDA reports)
CONSTIPATION ( 16 FDA reports)
DECREASED INTEREST ( 16 FDA reports)
DEFORMITY ( 16 FDA reports)
DYSAESTHESIA ( 16 FDA reports)
EMOTIONAL DISTRESS ( 16 FDA reports)
EPIDIDYMITIS ( 16 FDA reports)
ERECTILE DYSFUNCTION ( 16 FDA reports)
HYDROCELE ( 16 FDA reports)
HYPOAESTHESIA ( 16 FDA reports)
HYPOCALCAEMIA ( 16 FDA reports)
HYPOPHAGIA ( 16 FDA reports)
HYPOTENSION ( 16 FDA reports)
INFECTION ( 16 FDA reports)
INJURY ( 16 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 16 FDA reports)
LEFT ATRIAL DILATATION ( 16 FDA reports)
LEUKOCYTOSIS ( 16 FDA reports)
LIFE EXPECTANCY SHORTENED ( 16 FDA reports)
MUSCLE TWITCHING ( 16 FDA reports)
NEURALGIA ( 16 FDA reports)
OSTEOMYELITIS ( 16 FDA reports)
OSTEONECROSIS OF JAW ( 16 FDA reports)
PERIPHERAL EMBOLISM ( 16 FDA reports)
PNEUMONIA ( 16 FDA reports)
PRESYNCOPE ( 16 FDA reports)
PROTHROMBIN TIME PROLONGED ( 16 FDA reports)
PYREXIA ( 16 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
RENAL ISCHAEMIA ( 16 FDA reports)
SINUS TACHYCARDIA ( 16 FDA reports)
SINUSITIS ( 16 FDA reports)
SOMNOLENCE ( 16 FDA reports)
SPINAL OSTEOARTHRITIS ( 16 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
TACHYARRHYTHMIA ( 16 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 16 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
WHEEZING ( 16 FDA reports)
ABDOMINAL PAIN UPPER ( 15 FDA reports)
ANAEMIA ( 15 FDA reports)
ARTHRALGIA ( 15 FDA reports)
ONYCHOMYCOSIS ( 15 FDA reports)
PHLEBITIS ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
WEIGHT DECREASED ( 15 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 14 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 14 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 14 FDA reports)
HYPERLIPIDAEMIA ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 13 FDA reports)
LIBIDO DECREASED ( 13 FDA reports)
ORCHITIS ( 13 FDA reports)
PAIN IN JAW ( 13 FDA reports)
PLEURAL EFFUSION ( 13 FDA reports)
TESTICULAR PAIN ( 13 FDA reports)
TESTICULAR SWELLING ( 13 FDA reports)
BACK PAIN ( 12 FDA reports)
GYNAECOMASTIA ( 12 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
DIZZINESS ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
CONJUNCTIVITIS ( 10 FDA reports)
CORNEAL ABRASION ( 10 FDA reports)
GASTRITIS ( 10 FDA reports)
HYPOAESTHESIA FACIAL ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
DEBRIDEMENT ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
ALOPECIA ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
CATARACT ( 6 FDA reports)
DEATH ( 6 FDA reports)
FALL ( 6 FDA reports)
OPEN WOUND ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
INTERMITTENT CLAUDICATION ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
NAIL DYSTROPHY ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SKIN INJURY ( 5 FDA reports)
ACNE ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
VOMITING ( 4 FDA reports)
APRAXIA ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
KERATOACANTHOMA ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DELAYED SLEEP PHASE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PELVIC DISCOMFORT ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
POISONING ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)

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