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CROHN'S DISEASE ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
ILEUS ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
INTESTINAL STENOSIS ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PUSTULAR PSORIASIS ( 6 FDA reports)
CACHEXIA ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
COLITIS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ANORECTAL DISORDER ( 3 FDA reports)
CEREBRAL THROMBOSIS ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTENSIVE CARE ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MICROTIA ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
PAIN ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RASH ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 2 FDA reports)
FALL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INVESTIGATION ( 2 FDA reports)
IRIS COLOBOMA ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MICROPHTHALMOS ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ADRENAL ATROPHY ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JEJUNAL STENOSIS ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MAMMOPLASTY ( 1 FDA reports)
MASS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL ULCERATION ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)

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