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

PYREXIA ( 31 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 26 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 22 FDA reports)
HYPOTENSION ( 20 FDA reports)
PNEUMONIA ( 19 FDA reports)
PLEURAL EFFUSION ( 18 FDA reports)
HAEMOGLOBIN DECREASED ( 17 FDA reports)
DYSPNOEA ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
NAUSEA ( 13 FDA reports)
CHILLS ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
RENAL IMPAIRMENT ( 10 FDA reports)
VOMITING ( 10 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ANAEMIA ( 8 FDA reports)
ANXIETY ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
COUGH ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
LEUKOCYTOSIS ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
RESPIRATORY DEPRESSION ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DRUG DOSE OMISSION ( 6 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
INFUSION RELATED REACTION ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RETINOIC ACID SYNDROME ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
VISUAL DISTURBANCE ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COMA ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FALL ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
NEOPLASM PROGRESSION ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
RASH ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
AEROMONA INFECTION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BONE MARROW NECROSIS ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHLAMYDIA IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOSTASIS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RED BLOOD CELL ABNORMALITY ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITAMIN B1 DECREASED ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC TRANSFUSION REACTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYP ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)

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