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

HEPATIC FUNCTION ABNORMAL ( 180 FDA reports)
CARDIAC FAILURE ( 160 FDA reports)
PYREXIA ( 130 FDA reports)
INTERSTITIAL LUNG DISEASE ( 129 FDA reports)
LIVER DISORDER ( 118 FDA reports)
BLOOD CREATININE INCREASED ( 117 FDA reports)
DECREASED APPETITE ( 102 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 102 FDA reports)
PLATELET COUNT DECREASED ( 101 FDA reports)
BLOOD UREA INCREASED ( 99 FDA reports)
MALAISE ( 99 FDA reports)
RENAL FAILURE ACUTE ( 95 FDA reports)
RENAL IMPAIRMENT ( 94 FDA reports)
BLOOD PRESSURE DECREASED ( 92 FDA reports)
PNEUMONIA ( 89 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 87 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 82 FDA reports)
ANAEMIA ( 79 FDA reports)
VOMITING ( 78 FDA reports)
BRADYCARDIA ( 77 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 72 FDA reports)
HAEMOGLOBIN DECREASED ( 71 FDA reports)
HYPOGLYCAEMIA ( 70 FDA reports)
DYSPNOEA ( 68 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 66 FDA reports)
DRUG INTERACTION ( 64 FDA reports)
PLEURAL EFFUSION ( 64 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 63 FDA reports)
CEREBRAL INFARCTION ( 63 FDA reports)
DIZZINESS ( 63 FDA reports)
NAUSEA ( 62 FDA reports)
LOSS OF CONSCIOUSNESS ( 60 FDA reports)
RHABDOMYOLYSIS ( 60 FDA reports)
CONDITION AGGRAVATED ( 58 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 58 FDA reports)
DIARRHOEA ( 57 FDA reports)
RENAL FAILURE ( 50 FDA reports)
THROMBOCYTOPENIA ( 50 FDA reports)
DEHYDRATION ( 49 FDA reports)
HYPONATRAEMIA ( 49 FDA reports)
OEDEMA PERIPHERAL ( 49 FDA reports)
CARDIO-RESPIRATORY ARREST ( 48 FDA reports)
DYSARTHRIA ( 48 FDA reports)
HYPERKALAEMIA ( 48 FDA reports)
ASTHENIA ( 47 FDA reports)
HYPOTENSION ( 47 FDA reports)
RASH ( 47 FDA reports)
SOMNOLENCE ( 47 FDA reports)
ATRIAL FIBRILLATION ( 46 FDA reports)
BLOOD GLUCOSE INCREASED ( 46 FDA reports)
DEATH ( 46 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 46 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 46 FDA reports)
SHOCK ( 45 FDA reports)
HYPERTENSION ( 44 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 43 FDA reports)
AGRANULOCYTOSIS ( 42 FDA reports)
JAUNDICE ( 42 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 40 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 39 FDA reports)
FALL ( 39 FDA reports)
ANGINA PECTORIS ( 38 FDA reports)
HEADACHE ( 38 FDA reports)
OVERDOSE ( 38 FDA reports)
CARDIAC ARREST ( 36 FDA reports)
RENAL DISORDER ( 36 FDA reports)
STEVENS-JOHNSON SYNDROME ( 36 FDA reports)
DIABETES MELLITUS ( 35 FDA reports)
OEDEMA ( 35 FDA reports)
SEPSIS ( 35 FDA reports)
ARRHYTHMIA ( 34 FDA reports)
BLOOD POTASSIUM INCREASED ( 34 FDA reports)
MYOCARDIAL INFARCTION ( 33 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 33 FDA reports)
ANOREXIA ( 32 FDA reports)
CONVULSION ( 32 FDA reports)
COUGH ( 32 FDA reports)
HAEMATOCRIT DECREASED ( 32 FDA reports)
DRUG ERUPTION ( 31 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 31 FDA reports)
PANCYTOPENIA ( 31 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 30 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 30 FDA reports)
BLOOD PRESSURE INCREASED ( 29 FDA reports)
BLOOD URIC ACID INCREASED ( 28 FDA reports)
PRURITUS ( 28 FDA reports)
VENTRICULAR TACHYCARDIA ( 28 FDA reports)
ABDOMINAL PAIN ( 27 FDA reports)
GASTRIC ULCER ( 27 FDA reports)
URINE OUTPUT DECREASED ( 27 FDA reports)
WEIGHT INCREASED ( 27 FDA reports)
EOSINOPHIL COUNT INCREASED ( 26 FDA reports)
HAEMODIALYSIS ( 26 FDA reports)
INFECTION ( 26 FDA reports)
RENAL FAILURE CHRONIC ( 26 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 26 FDA reports)
DELIRIUM ( 25 FDA reports)
NEUTROPENIA ( 25 FDA reports)
NEUTROPHIL COUNT DECREASED ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 24 FDA reports)
CHEST PAIN ( 24 FDA reports)
FEELING ABNORMAL ( 24 FDA reports)
LUNG DISORDER ( 24 FDA reports)
SUICIDE ATTEMPT ( 24 FDA reports)
FATIGUE ( 23 FDA reports)
HAEMORRHAGE ( 23 FDA reports)
HEART RATE DECREASED ( 23 FDA reports)
NASOPHARYNGITIS ( 23 FDA reports)
CARDIOMEGALY ( 22 FDA reports)
HEPATIC ENZYME INCREASED ( 22 FDA reports)
LEUKOPENIA ( 22 FDA reports)
PYELONEPHRITIS ( 22 FDA reports)
URINARY TRACT INFECTION ( 22 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 21 FDA reports)
CARDIAC FAILURE CHRONIC ( 21 FDA reports)
CEREBRAL HAEMORRHAGE ( 21 FDA reports)
FACE OEDEMA ( 21 FDA reports)
HEPATITIS FULMINANT ( 21 FDA reports)
PULMONARY CONGESTION ( 21 FDA reports)
WEIGHT DECREASED ( 21 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 20 FDA reports)
GAIT DISTURBANCE ( 20 FDA reports)
HEPATIC FAILURE ( 20 FDA reports)
HYPOAESTHESIA ( 20 FDA reports)
ANAPHYLACTIC SHOCK ( 19 FDA reports)
CONSTIPATION ( 19 FDA reports)
ENCEPHALOPATHY ( 19 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 19 FDA reports)
BACK PAIN ( 18 FDA reports)
CHEST DISCOMFORT ( 18 FDA reports)
CHILLS ( 18 FDA reports)
DYSLALIA ( 18 FDA reports)
EOSINOPHILIA ( 18 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 18 FDA reports)
HAEMOPTYSIS ( 18 FDA reports)
HYPERGLYCAEMIA ( 18 FDA reports)
HYPERHIDROSIS ( 18 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 18 FDA reports)
MULTI-ORGAN FAILURE ( 18 FDA reports)
PROTHROMBIN TIME PROLONGED ( 18 FDA reports)
RASH GENERALISED ( 18 FDA reports)
RESPIRATORY ARREST ( 18 FDA reports)
ANURIA ( 17 FDA reports)
BONE MARROW FAILURE ( 17 FDA reports)
DRUG HYPERSENSITIVITY ( 17 FDA reports)
ERYTHEMA ( 17 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 17 FDA reports)
RESTLESSNESS ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
BLOOD BILIRUBIN INCREASED ( 16 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 16 FDA reports)
DYSSTASIA ( 16 FDA reports)
HYPOPHAGIA ( 16 FDA reports)
MELAENA ( 16 FDA reports)
MUSCULAR WEAKNESS ( 16 FDA reports)
PULMONARY OEDEMA ( 16 FDA reports)
STOMATITIS ( 16 FDA reports)
VENTRICULAR FIBRILLATION ( 16 FDA reports)
ARTHRALGIA ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 15 FDA reports)
CARDIAC FAILURE ACUTE ( 15 FDA reports)
COMA ( 15 FDA reports)
DYSPNOEA EXERTIONAL ( 15 FDA reports)
OXYGEN SATURATION DECREASED ( 15 FDA reports)
PROTEIN TOTAL DECREASED ( 15 FDA reports)
PULMONARY HYPERTENSION ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
BLOOD POTASSIUM DECREASED ( 14 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 14 FDA reports)
HYPOKALAEMIA ( 14 FDA reports)
OESOPHAGEAL ULCER ( 14 FDA reports)
TREMOR ( 14 FDA reports)
ABDOMINAL DISTENSION ( 13 FDA reports)
DISCOMFORT ( 13 FDA reports)
HOT FLUSH ( 13 FDA reports)
HYPOGLYCAEMIC COMA ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
MYOCARDIAL ISCHAEMIA ( 13 FDA reports)
NERVOUS SYSTEM DISORDER ( 13 FDA reports)
OLIGURIA ( 13 FDA reports)
SICK SINUS SYNDROME ( 13 FDA reports)
SWELLING ( 13 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 12 FDA reports)
BLOOD AMYLASE INCREASED ( 12 FDA reports)
CHOLECYSTITIS ( 12 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 12 FDA reports)
DIALYSIS ( 12 FDA reports)
GASTROINTESTINAL TOXICITY ( 12 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 12 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 12 FDA reports)
PAIN ( 12 FDA reports)
PNEUMONIA BACTERIAL ( 12 FDA reports)
PSYCHIATRIC SYMPTOM ( 12 FDA reports)
SURGERY ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 12 FDA reports)
ABDOMINAL PAIN UPPER ( 11 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 11 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 11 FDA reports)
BLOOD GLUCOSE DECREASED ( 11 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 11 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 11 FDA reports)
CONJUNCTIVITIS ( 11 FDA reports)
EPISTAXIS ( 11 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 11 FDA reports)
HAEMATEMESIS ( 11 FDA reports)
HEPATOCELLULAR INJURY ( 11 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 11 FDA reports)
HYPERTHERMIA ( 11 FDA reports)
LUNG NEOPLASM MALIGNANT ( 11 FDA reports)
METABOLIC ACIDOSIS ( 11 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 11 FDA reports)
ORTHOPNOEA ( 11 FDA reports)
OSTEOMYELITIS ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
PHLEBITIS ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
PYELONEPHRITIS ACUTE ( 11 FDA reports)
RENAL CYST ( 11 FDA reports)
SUDDEN DEATH ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
ABASIA ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ATRIOVENTRICULAR BLOCK ( 10 FDA reports)
BLOOD ALBUMIN DECREASED ( 10 FDA reports)
BODY TEMPERATURE DECREASED ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
CEREBELLAR HAEMORRHAGE ( 10 FDA reports)
CHOLESTASIS ( 10 FDA reports)
COLD SWEAT ( 10 FDA reports)
CORONARY ARTERY OCCLUSION ( 10 FDA reports)
CORONARY ARTERY RESTENOSIS ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 10 FDA reports)
GASTROENTERITIS ( 10 FDA reports)
GRANULOCYTE COUNT DECREASED ( 10 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 10 FDA reports)
HALLUCINATION ( 10 FDA reports)
HEMIPLEGIA ( 10 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 10 FDA reports)
HYPOTHYROIDISM ( 10 FDA reports)
LYMPHOPENIA ( 10 FDA reports)
PANCREATITIS ACUTE ( 10 FDA reports)
PERITONITIS ( 10 FDA reports)
PLATELET COUNT INCREASED ( 10 FDA reports)
PRURITUS GENERALISED ( 10 FDA reports)
RENAL TUBULAR DISORDER ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
SUBDURAL HAEMATOMA ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
BLOOD CHLORIDE DECREASED ( 9 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 9 FDA reports)
BONE DISORDER ( 9 FDA reports)
BRONCHIOLITIS ( 9 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CARDIAC PACEMAKER INSERTION ( 9 FDA reports)
CHROMATURIA ( 9 FDA reports)
CORONARY ARTERY STENOSIS ( 9 FDA reports)
GRANULOCYTOPENIA ( 9 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
APHASIA ( 8 FDA reports)
ASTHMA ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
CORTICAL LAMINAR NECROSIS ( 8 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 8 FDA reports)
GALLBLADDER ENLARGEMENT ( 8 FDA reports)
GASTRIC CANCER ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
HAEMORRHAGIC INFARCTION ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
LARGE INTESTINE CARCINOMA ( 8 FDA reports)
LARGE INTESTINE PERFORATION ( 8 FDA reports)
MYOGLOBINURIA ( 8 FDA reports)
OSTEOPOROSIS ( 8 FDA reports)
PALLOR ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
REHABILITATION THERAPY ( 8 FDA reports)
SCAR ( 8 FDA reports)
SINUS BRADYCARDIA ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
THROMBOSIS IN DEVICE ( 8 FDA reports)
TONIC CONVULSION ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ANGINA UNSTABLE ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
ASCITES ( 7 FDA reports)
BACTERIAL INFECTION ( 7 FDA reports)
BLISTER ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
ELECTROLYTE IMBALANCE ( 7 FDA reports)
ENDOTRACHEAL INTUBATION ( 7 FDA reports)
FAECES DISCOLOURED ( 7 FDA reports)
GASTRIC NEOPLASM ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
ILL-DEFINED DISORDER ( 7 FDA reports)
INFUSION RELATED REACTION ( 7 FDA reports)
INJECTION SITE INDURATION ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
NEPHROPATHY TOXIC ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
OESOPHAGEAL NEOPLASM ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PURPURA ( 7 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
SINUS ARREST ( 7 FDA reports)
STENT PLACEMENT ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
ACIDOSIS ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
EJECTION FRACTION DECREASED ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
ESCHERICHIA SEPSIS ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
ILEUS ( 6 FDA reports)
INTRACARDIAC THROMBUS ( 6 FDA reports)
MALABSORPTION ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PULSE ABSENT ( 6 FDA reports)
TACHYPNOEA ( 6 FDA reports)
THROAT TIGHTNESS ( 6 FDA reports)
TONSILLITIS ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
WOUND ( 6 FDA reports)
ABSCESS ( 5 FDA reports)
ABSCESS DRAINAGE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
AZOTAEMIA ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD URINE PRESENT ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CELL MARKER INCREASED ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 5 FDA reports)
CHOKING ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIABETIC ENTEROPATHY ( 5 FDA reports)
DIABETIC KETOACIDOSIS ( 5 FDA reports)
DIZZINESS POSTURAL ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
EYELID FUNCTION DISORDER ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FEELING COLD ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 5 FDA reports)
GASTRIC ADENOMA ( 5 FDA reports)
GASTRIC MUCOSAL LESION ( 5 FDA reports)
GINGIVAL ERYTHEMA ( 5 FDA reports)
GINGIVAL SWELLING ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HYPERBILIRUBINAEMIA ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 5 FDA reports)
LACUNAR INFARCTION ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
PRIMARY SEQUESTRUM ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PULMONARY TUBERCULOSIS ( 5 FDA reports)
RENAL ATROPHY ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SEQUESTRECTOMY ( 5 FDA reports)
SINOATRIAL BLOCK ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ABSCESS JAW ( 4 FDA reports)
ALCOHOL USE ( 4 FDA reports)
ALVEOLITIS ALLERGIC ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 4 FDA reports)
BLOOD INSULIN INCREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
BRONCHOSTENOSIS ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CLONIC CONVULSION ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COLITIS COLLAGENOUS ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DIABETIC NEPHROPATHY ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
FIBRIN INCREASED ( 4 FDA reports)
FISTULA ( 4 FDA reports)
GASTRIC LAVAGE ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GLOSSOPTOSIS ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HAEMOSTASIS ( 4 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPERTHERMIA MALIGNANT ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE WARMTH ( 4 FDA reports)
INTESTINAL DILATATION ( 4 FDA reports)
JAW LESION EXCISION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
MICTURITION FREQUENCY DECREASED ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MOUTH BREATHING ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OESOPHAGEAL CARCINOMA ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
OSTEOMALACIA ( 4 FDA reports)
OXYGEN SUPPLEMENTATION ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PARONYCHIA ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 4 FDA reports)
PUTAMEN HAEMORRHAGE ( 4 FDA reports)
RALES ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RENAL GRAFT LOSS ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VOLUME BLOOD INCREASED ( 4 FDA reports)
WOUND HAEMORRHAGE ( 4 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ALBUMIN URINE ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
BIOPSY PROSTATE ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD URIC ACID DECREASED ( 3 FDA reports)
BRAIN CONTUSION ( 3 FDA reports)
BRAIN MASS ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC MASSAGE ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATHETERISATION CARDIAC ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CORONARY ARTERY THROMBOSIS ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 3 FDA reports)
OROPHARYNGITIS FUNGAL ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
YAWNING ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
AORTIC DISSECTION RUPTURE ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BONE ATROPHY ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CROSS SENSITIVITY REACTION ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIALYSIS DEVICE INSERTION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORDER OF GLOBE ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
EOSINOPHILIC FASCIITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPERVITAMINOSIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MELANODERMIA ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PALATAL DISORDER ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLASMA CELL COUNT ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULSE ABNORMAL ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DYSKINESIA ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ULNAR NEURITIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTI-INSULIN ANTIBODY ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEST WALL OPERATION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLSTONES IN BILE DUCT REMOVAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
NASAL MUCOSA ATROPHY ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL MUCOSA ATROPHY ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERICORONITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBIN TIME ABNORMAL ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)

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