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

JAUNDICE ( 20 FDA reports)
PNEUMONIA ( 14 FDA reports)
DEHYDRATION ( 13 FDA reports)
DIARRHOEA ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
VOMITING ( 10 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 9 FDA reports)
DEATH ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
PSORIASIS ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
FALL ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HYPERCALCAEMIA ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIORENAL SYNDROME ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LYMPHANGITIS ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
OBESITY ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SNORING ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN TOXICITY ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TETANY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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