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

PYREXIA ( 47 FDA reports)
RASH ( 40 FDA reports)
ANAEMIA ( 36 FDA reports)
PLATELET COUNT DECREASED ( 33 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 31 FDA reports)
STOMATITIS ( 28 FDA reports)
DECREASED APPETITE ( 26 FDA reports)
INTERSTITIAL LUNG DISEASE ( 23 FDA reports)
ERYTHEMA ( 22 FDA reports)
DRUG ERUPTION ( 20 FDA reports)
HAEMOGLOBIN DECREASED ( 20 FDA reports)
PRURITUS ( 20 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 20 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
INFECTION ( 17 FDA reports)
DERMATITIS ACNEIFORM ( 16 FDA reports)
LIVER DISORDER ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 16 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 14 FDA reports)
RENAL DISORDER ( 14 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 12 FDA reports)
ERYTHEMA MULTIFORME ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
ASCITES ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
HEPATITIS C ( 11 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 10 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 10 FDA reports)
BURSITIS ( 10 FDA reports)
DERMATITIS EXFOLIATIVE ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
PLEURAL INFECTION BACTERIAL ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
PNEUMONIA BACTERIAL ( 10 FDA reports)
RASH PUSTULAR ( 10 FDA reports)
SHOCK ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
DIABETES MELLITUS ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
INTERNAL HERNIA ( 9 FDA reports)
INTESTINAL PERFORATION ( 9 FDA reports)
JAUNDICE ( 9 FDA reports)
MECHANICAL ILEUS ( 9 FDA reports)
NEUTROPHIL COUNT DECREASED ( 9 FDA reports)
SEPTIC SHOCK ( 9 FDA reports)
ANURIA ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
MENINGITIS BACTERIAL ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
COUGH ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 7 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 7 FDA reports)
MALAISE ( 7 FDA reports)
METASTASES TO LIVER ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 7 FDA reports)
SURGERY ( 7 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
CHILLS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
FIBRIN D DIMER INCREASED ( 6 FDA reports)
FIBRIN DECREASED ( 6 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 6 FDA reports)
GASTRIC HAEMORRHAGE ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 6 FDA reports)
MELAENA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
RETICULOCYTE COUNT INCREASED ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INFUSION RELATED REACTION ( 5 FDA reports)
METASTATIC PAIN ( 5 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PARONYCHIA ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
SELECTIVE ABORTION ( 5 FDA reports)
SKIN LESION ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLOOD CHLORIDE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
ENANTHEMA ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OVARIAN CANCER RECURRENT ( 4 FDA reports)
PAIN ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PUSTULAR PSORIASIS ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
ACNE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BLOOD BILIRUBIN DECREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
COLORECTAL CANCER ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FAMILIAL MEDITERRANEAN FEVER ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
OBESITY ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
SCLERODERMA RENAL CRISIS ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TONGUE ERUPTION ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
IMMINENT ABORTION ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
TONSIL CANCER ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VULVAR EROSION ( 2 FDA reports)
ABORTION ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BED REST ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)

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