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

DIARRHOEA ( 26 FDA reports)
RENAL FAILURE ( 26 FDA reports)
DYSPNOEA ( 24 FDA reports)
PYREXIA ( 24 FDA reports)
VOMITING ( 22 FDA reports)
FATIGUE ( 20 FDA reports)
NAUSEA ( 19 FDA reports)
ASTHENIA ( 18 FDA reports)
ANAEMIA ( 16 FDA reports)
MYOCARDIAL INFARCTION ( 16 FDA reports)
DECREASED APPETITE ( 15 FDA reports)
OSTEONECROSIS ( 15 FDA reports)
URINARY TRACT INFECTION ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
FALL ( 14 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 14 FDA reports)
OEDEMA PERIPHERAL ( 14 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
HYPERTENSION ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
COUGH ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
VERTIGO ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CROHN'S DISEASE ( 9 FDA reports)
DEATH ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
INFECTION ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
EMPHYSEMA ( 8 FDA reports)
FAECALOMA ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CHILLS ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
TOOTH EXTRACTION ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
NEPHRITIS INTERSTITIAL ( 6 FDA reports)
PAIN ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RASH ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIOVERSION ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEPATITIS TOXIC ( 5 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
PANNICULITIS ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
STRESS ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BLOOD PROLACTIN INCREASED ( 4 FDA reports)
BRAIN HYPOXIA ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CATHETER THROMBOSIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
CYTOTOXIC OEDEMA ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERTROPHY BREAST ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPERVISCOSITY SYNDROME ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PRIMARY SEQUESTRUM ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TREMOR ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
AMYOTROPHY ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASEPTIC NECROSIS BONE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLOOD CORTISOL INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHOPNEUMOPATHY ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
COMA ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GOUT ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MACROCYTOSIS ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 3 FDA reports)
OROPHARYNGEAL PLAQUE ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
STASIS DERMATITIS ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
URINARY BLADDER POLYP ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VITAMIN D DECREASED ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ABSCESS ORAL ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BONE LESION EXCISION ( 2 FDA reports)
BONE MARROW OEDEMA ( 2 FDA reports)
BONE OPERATION ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC VALVE VEGETATION ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEMENTIA OF THE ALZHEIMER'S TYPE, WITH DELIRIUM ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FISTULA ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIGAMENT RUPTURE ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE RUPTURE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEURILEMMOMA ( 2 FDA reports)
NEUROPATHIC ARTHROPATHY ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TONGUE NEOPLASM ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLADDER NECK SCLEROSIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HANTAVIRAL INFECTION ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIC BLADDER ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
ILEAL ULCER PERFORATION ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
MASS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XEROPHTHALMIA ( 1 FDA reports)

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