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

VOMITING ( 26 FDA reports)
NAUSEA ( 22 FDA reports)
DRUG INTERACTION ( 21 FDA reports)
DEHYDRATION ( 19 FDA reports)
DYSPNOEA ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
MUSCULAR WEAKNESS ( 13 FDA reports)
RHABDOMYOLYSIS ( 12 FDA reports)
HYPERKALAEMIA ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
FALL ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
AGITATION ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
SEROTONIN SYNDROME ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
INJECTION SITE DISCOLOURATION ( 6 FDA reports)
JOINT INJURY ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
RENAL TRANSPLANT ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ACIDOSIS ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ATRIAL SEPTAL DEFECT ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
COUGH ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
PAIN ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COMA ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
MELAENA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PROSTRATION ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SURGERY ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATOFIBROSARCOMA ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SALPINGECTOMY ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

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