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

CARDIAC FAILURE ( 249 FDA reports)
DYSPNOEA ( 234 FDA reports)
HYPOTENSION ( 151 FDA reports)
DISEASE PROGRESSION ( 147 FDA reports)
BLOOD CREATININE INCREASED ( 138 FDA reports)
RENAL IMPAIRMENT ( 133 FDA reports)
ATRIAL FIBRILLATION ( 118 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 112 FDA reports)
DECREASED APPETITE ( 111 FDA reports)
MALAISE ( 110 FDA reports)
OEDEMA PERIPHERAL ( 93 FDA reports)
ABDOMINAL PAIN ( 89 FDA reports)
DIZZINESS ( 88 FDA reports)
DEHYDRATION ( 84 FDA reports)
DRUG INEFFECTIVE ( 82 FDA reports)
CHEST PAIN ( 81 FDA reports)
RENAL FAILURE ( 80 FDA reports)
DEATH ( 75 FDA reports)
HYPERKALAEMIA ( 69 FDA reports)
CONDITION AGGRAVATED ( 68 FDA reports)
NAUSEA ( 68 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 66 FDA reports)
PNEUMONIA ( 64 FDA reports)
ASTHENIA ( 63 FDA reports)
PROSTATE CANCER ( 63 FDA reports)
PYREXIA ( 63 FDA reports)
BLOOD PRESSURE INCREASED ( 62 FDA reports)
RENAL FAILURE ACUTE ( 61 FDA reports)
SYNCOPE ( 61 FDA reports)
ANGINA PECTORIS ( 59 FDA reports)
HYPERTENSION ( 58 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 58 FDA reports)
VOMITING ( 55 FDA reports)
FALL ( 54 FDA reports)
CARDIAC FAILURE ACUTE ( 52 FDA reports)
DIARRHOEA ( 51 FDA reports)
FATIGUE ( 50 FDA reports)
OEDEMA ( 50 FDA reports)
BLOOD UREA INCREASED ( 48 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 47 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 47 FDA reports)
HAEMOGLOBIN DECREASED ( 47 FDA reports)
HYPONATRAEMIA ( 47 FDA reports)
BLOOD GLUCOSE INCREASED ( 46 FDA reports)
COUGH ( 46 FDA reports)
CEREBRAL INFARCTION ( 45 FDA reports)
FACE OEDEMA ( 45 FDA reports)
PLEURAL EFFUSION ( 45 FDA reports)
RENAL FAILURE CHRONIC ( 44 FDA reports)
BLOOD POTASSIUM INCREASED ( 43 FDA reports)
WEIGHT INCREASED ( 43 FDA reports)
ANAEMIA ( 42 FDA reports)
CORONARY ARTERY DISEASE ( 42 FDA reports)
ABDOMINAL DISTENSION ( 40 FDA reports)
ASTHMA ( 40 FDA reports)
CARDIAC FAILURE CHRONIC ( 34 FDA reports)
CEREBROVASCULAR ACCIDENT ( 34 FDA reports)
ABDOMINAL DISCOMFORT ( 33 FDA reports)
ABDOMINAL PAIN UPPER ( 31 FDA reports)
HAEMATOCRIT DECREASED ( 31 FDA reports)
HEADACHE ( 31 FDA reports)
HYPOGLYCAEMIA ( 31 FDA reports)
HYPOPHAGIA ( 31 FDA reports)
BLOOD PRESSURE DECREASED ( 30 FDA reports)
GASTRIC ULCER ( 30 FDA reports)
HEPATITIS ACUTE ( 30 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 29 FDA reports)
CONSTIPATION ( 29 FDA reports)
DYSPNOEA EXERTIONAL ( 29 FDA reports)
HEMIPARESIS ( 29 FDA reports)
CHOLELITHIASIS ( 28 FDA reports)
MUSCULOSKELETAL PAIN ( 28 FDA reports)
URINARY TRACT INFECTION ( 28 FDA reports)
CARDIOMEGALY ( 27 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 27 FDA reports)
DIABETES MELLITUS ( 27 FDA reports)
JOINT SWELLING ( 27 FDA reports)
ORTHOPNOEA ( 27 FDA reports)
PALLOR ( 27 FDA reports)
PULMONARY OEDEMA ( 27 FDA reports)
MYOCARDIAL INFARCTION ( 26 FDA reports)
MYOCARDIAL ISCHAEMIA ( 26 FDA reports)
VERTIGO ( 26 FDA reports)
BACK PAIN ( 25 FDA reports)
BURNING SENSATION ( 25 FDA reports)
OESOPHAGEAL ULCER ( 25 FDA reports)
VENTRICULAR TACHYCARDIA ( 25 FDA reports)
ANKLE FRACTURE ( 24 FDA reports)
BONE ATROPHY ( 24 FDA reports)
EYELID OEDEMA ( 24 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 24 FDA reports)
HEART RATE DECREASED ( 24 FDA reports)
METASTASIS ( 24 FDA reports)
OCULAR ICTERUS ( 24 FDA reports)
ROTATOR CUFF SYNDROME ( 24 FDA reports)
SWELLING ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 23 FDA reports)
BRADYCARDIA ( 22 FDA reports)
CHILLS ( 22 FDA reports)
DEPRESSION ( 22 FDA reports)
DRUG INTERACTION ( 22 FDA reports)
HYPERTENSIVE CRISIS ( 22 FDA reports)
LOSS OF CONSCIOUSNESS ( 22 FDA reports)
RHABDOMYOLYSIS ( 22 FDA reports)
CARDIAC ARREST ( 21 FDA reports)
CHEST DISCOMFORT ( 21 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 21 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 21 FDA reports)
VENTRICULAR FIBRILLATION ( 21 FDA reports)
ABDOMINAL PAIN LOWER ( 20 FDA reports)
ANGIOEDEMA ( 20 FDA reports)
CELLULITIS ( 20 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 20 FDA reports)
PAIN ( 20 FDA reports)
PAIN IN EXTREMITY ( 20 FDA reports)
SUDDEN CARDIAC DEATH ( 20 FDA reports)
WEIGHT DECREASED ( 20 FDA reports)
ARTHRALGIA ( 19 FDA reports)
HEART RATE INCREASED ( 19 FDA reports)
PULMONARY CONGESTION ( 19 FDA reports)
RALES ( 19 FDA reports)
SEPSIS ( 19 FDA reports)
ACUTE PULMONARY OEDEMA ( 18 FDA reports)
CONFUSIONAL STATE ( 18 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 18 FDA reports)
GASTRIC CANCER ( 18 FDA reports)
TACHYCARDIA ( 18 FDA reports)
BLOOD POTASSIUM DECREASED ( 17 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 17 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 17 FDA reports)
CARDIO-RESPIRATORY ARREST ( 17 FDA reports)
GASTRIC NEOPLASM ( 17 FDA reports)
HYPERGLYCAEMIA ( 17 FDA reports)
INFECTION ( 17 FDA reports)
OESOPHAGEAL NEOPLASM ( 17 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 16 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
ARRHYTHMIA ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK ( 15 FDA reports)
DYSPNOEA AT REST ( 15 FDA reports)
PULMONARY HYPERTENSION ( 15 FDA reports)
ATRIAL FLUTTER ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
DIABETIC NEPHROPATHY ( 14 FDA reports)
FEELING COLD ( 14 FDA reports)
GASTRITIS ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPERURICAEMIA ( 14 FDA reports)
HYPOKALAEMIA ( 14 FDA reports)
NEPHROTIC SYNDROME ( 14 FDA reports)
PRODUCTIVE COUGH ( 14 FDA reports)
PRURITUS ( 14 FDA reports)
RENAL CELL CARCINOMA ( 14 FDA reports)
RENAL CYST ( 14 FDA reports)
STAPHYLOCOCCAL INFECTION ( 14 FDA reports)
DIABETIC KETOACIDOSIS ( 13 FDA reports)
FAECES DISCOLOURED ( 13 FDA reports)
RASH ( 13 FDA reports)
SPINAL COLUMN STENOSIS ( 13 FDA reports)
SUDDEN DEATH ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 12 FDA reports)
DYSURIA ( 12 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 12 FDA reports)
FLUID OVERLOAD ( 12 FDA reports)
GOUT ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
PRESYNCOPE ( 12 FDA reports)
PYELONEPHRITIS ACUTE ( 12 FDA reports)
SICK SINUS SYNDROME ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
ACUTE RESPIRATORY FAILURE ( 11 FDA reports)
ARTERIOSCLEROSIS ( 11 FDA reports)
BLOOD URIC ACID INCREASED ( 11 FDA reports)
CAROTID ARTERY STENOSIS ( 11 FDA reports)
COLON ADENOMA ( 11 FDA reports)
COLONIC POLYP ( 11 FDA reports)
DYSLALIA ( 11 FDA reports)
EJECTION FRACTION DECREASED ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 11 FDA reports)
MYELOPATHY ( 11 FDA reports)
PARESIS ( 11 FDA reports)
PROTEINURIA ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
RIGHT VENTRICULAR FAILURE ( 11 FDA reports)
STREPTOCOCCAL INFECTION ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 10 FDA reports)
CARDIAC PACEMAKER INSERTION ( 10 FDA reports)
GASTROENTERITIS ( 10 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 10 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
POLLAKIURIA ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
ROAD TRAFFIC ACCIDENT ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
BLOOD GLUCOSE DECREASED ( 9 FDA reports)
CARDIOGENIC SHOCK ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
CORONARY ARTERY OCCLUSION ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 9 FDA reports)
LUNG INFECTION ( 9 FDA reports)
LUNG NEOPLASM MALIGNANT ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
PERIPHERAL COLDNESS ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
VOLUME BLOOD INCREASED ( 9 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BRAIN OEDEMA ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CATHETERISATION CARDIAC ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
CORONARY ARTERY RESTENOSIS ( 8 FDA reports)
CORTICAL LAMINAR NECROSIS ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
GALLBLADDER ENLARGEMENT ( 8 FDA reports)
GASTRITIS ATROPHIC ( 8 FDA reports)
HAEMATURIA ( 8 FDA reports)
HAEMORRHAGIC INFARCTION ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 8 FDA reports)
INFLUENZA LIKE ILLNESS ( 8 FDA reports)
OSTEOARTHRITIS ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PERICARDITIS ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
POOR PERIPHERAL CIRCULATION ( 8 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
SCAR ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
SPUTUM RETENTION ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
WOUND COMPLICATION ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
BLADDER CANCER ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
CHOLECYSTITIS ( 7 FDA reports)
COMA ( 7 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 7 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
FEMORAL NECK FRACTURE ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
HALLUCINATION ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
LUNG CANCER METASTATIC ( 7 FDA reports)
MICROALBUMINURIA ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
TACHYPNOEA ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ACUTE ABDOMEN ( 6 FDA reports)
ANGINA UNSTABLE ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
APPENDICITIS ( 6 FDA reports)
APPENDICITIS PERFORATED ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CARDIOVERSION ( 6 FDA reports)
CHOLANGITIS ( 6 FDA reports)
CHOLECYSTITIS ACUTE ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GASTRITIS EROSIVE ( 6 FDA reports)
HEAT ILLNESS ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
ILEUS ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
ISCHAEMIC STROKE ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
OBESITY ( 6 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RENAL ARTERY STENOSIS ( 6 FDA reports)
TONIC CLONIC MOVEMENTS ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
APATHY ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD SODIUM INCREASED ( 5 FDA reports)
CEREBELLAR HAEMORRHAGE ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 5 FDA reports)
CORONARY ANGIOPLASTY ( 5 FDA reports)
CREATININE URINE INCREASED ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GASTRIC ADENOMA ( 5 FDA reports)
GASTRIC MUCOSAL LESION ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HUMERUS FRACTURE ( 5 FDA reports)
LISTLESS ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
OESOPHAGEAL CARCINOMA ( 5 FDA reports)
OESOPHAGEAL STENOSIS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PULMONARY MASS ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ADENOCARCINOMA ( 4 FDA reports)
ALCOHOL ABUSE ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 4 FDA reports)
BRAIN STEM INFARCTION ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
BUNDLE BRANCH BLOCK ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
DIABETIC GASTROPARESIS ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
DIVERTICULUM INTESTINAL ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DUODENAL NEOPLASM ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EMBOLISM ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HEART DISEASE CONGENITAL ( 4 FDA reports)
HEPATIC CALCIFICATION ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
ICHTHYOSIS ( 4 FDA reports)
INCREASED TENDENCY TO BRUISE ( 4 FDA reports)
INGUINAL HERNIA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
LIPIDS ABNORMAL ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
PANCREATIC CARCINOMA ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARTIAL SEIZURES ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
THIRST ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BILIRUBINURIA ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BULIMIA NERVOSA ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CEREBELLAR HAEMANGIOMA ( 3 FDA reports)
CEREBRAL HYPOPERFUSION ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY BYPASS ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 3 FDA reports)
GASTRIC INFECTION ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 3 FDA reports)
MESENTERIC ARTERY STENOSIS ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL CORD INJURY CERVICAL ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
THALAMIC INFARCTION ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALLERGIC HEPATITIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLADDER GRANULOMA ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRAIN STEM ISCHAEMIA ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIAL CARCINOMA ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETERISATION VENOUS ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTOSTOMY ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FILARIASIS ( 2 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
LARYNGEAL CANCER ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOEDEMA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYOCARDIAL FIBROSIS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORCHIDECTOMY ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PEPTIC ULCER PERFORATION ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 2 FDA reports)
PROSTATECTOMY ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RECTAL CANCER METASTATIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCIATIC NERVE INJURY ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TONGUE HAEMATOMA ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
URAEMIC ENCEPHALOPATHY ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE CALCIUM INCREASED ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WITHDRAWAL HYPERTENSION ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOVASCULAR EVENT PROPHYLAXIS ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTATIN C INCREASED ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HANTAVIRAL INFECTION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPOSARCOMA METASTATIC ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOPLASTY ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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