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

PNEUMONIA ( 30 FDA reports)
OVERDOSE ( 24 FDA reports)
HYPOTENSION ( 23 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 21 FDA reports)
RENAL FAILURE ACUTE ( 20 FDA reports)
ASTHENIA ( 19 FDA reports)
CELLULITIS ( 19 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
SYNCOPE ( 17 FDA reports)
ISCHAEMIC STROKE ( 16 FDA reports)
TREMOR ( 16 FDA reports)
URINARY TRACT INFECTION ( 16 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 15 FDA reports)
HYPOXIA ( 15 FDA reports)
HAEMATURIA ( 14 FDA reports)
HICCUPS ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 13 FDA reports)
DIZZINESS ( 13 FDA reports)
PERIPHERAL EMBOLISM ( 13 FDA reports)
BRONCHOPNEUMONIA ( 12 FDA reports)
CHOLELITHIASIS ( 12 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
OROPHARYNGEAL PAIN ( 12 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
CHOLECYSTITIS ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
HAEMORRHAGIC STROKE ( 11 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
COMA ( 8 FDA reports)
METASTATIC NEOPLASM ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
SUBDURAL HAEMATOMA ( 8 FDA reports)
ACCIDENTAL OVERDOSE ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
INTENTIONAL DRUG MISUSE ( 7 FDA reports)
PRESYNCOPE ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
AORTIC ANEURYSM RUPTURE ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
FALL ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
VOMITING ( 6 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
NON-CARDIAC CHEST PAIN ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 5 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
BACTERIAL DISEASE CARRIER ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DIVERTICULITIS ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 4 FDA reports)
MICROCYTIC ANAEMIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PAIN ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
DEATH ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GILBERT'S SYNDROME ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SMALL CELL CARCINOMA ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC DISSECTION RUPTURE ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOROIDAL HAEMORRHAGE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROOCULOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MORGANELLA TEST POSITIVE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORCHITIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER STAGE III ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOSOMATIC DISEASE ( 1 FDA reports)
PULMONARY AMYLOIDOSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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