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

DRUG INEFFECTIVE ( 61 FDA reports)
NAUSEA ( 43 FDA reports)
ASTHENIA ( 42 FDA reports)
OEDEMA PERIPHERAL ( 40 FDA reports)
HYPERTENSION ( 36 FDA reports)
MALAISE ( 36 FDA reports)
DIZZINESS ( 33 FDA reports)
FATIGUE ( 32 FDA reports)
DIARRHOEA ( 28 FDA reports)
DRUG INTERACTION ( 28 FDA reports)
VOMITING ( 28 FDA reports)
RENAL FAILURE ACUTE ( 27 FDA reports)
PAIN ( 26 FDA reports)
PYREXIA ( 26 FDA reports)
DEPRESSION ( 25 FDA reports)
ARTHRALGIA ( 24 FDA reports)
ANAEMIA ( 21 FDA reports)
FALL ( 21 FDA reports)
FEELING ABNORMAL ( 21 FDA reports)
PAIN IN EXTREMITY ( 21 FDA reports)
CONSTIPATION ( 20 FDA reports)
BLOOD PRESSURE INCREASED ( 19 FDA reports)
CHEST PAIN ( 19 FDA reports)
DEATH ( 19 FDA reports)
DYSPNOEA ( 19 FDA reports)
ANXIETY ( 18 FDA reports)
GAIT DISTURBANCE ( 18 FDA reports)
HEADACHE ( 18 FDA reports)
RENAL FAILURE ( 18 FDA reports)
WEIGHT DECREASED ( 18 FDA reports)
DEHYDRATION ( 17 FDA reports)
INTERSTITIAL LUNG DISEASE ( 17 FDA reports)
SOMNOLENCE ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
COUGH ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
AGGRESSION ( 15 FDA reports)
JOINT SWELLING ( 15 FDA reports)
RASH ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPOTENSION ( 14 FDA reports)
INSOMNIA ( 14 FDA reports)
MUSCULAR WEAKNESS ( 14 FDA reports)
PNEUMONIA ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
VISION BLURRED ( 14 FDA reports)
ABNORMAL DREAMS ( 13 FDA reports)
MUSCLE SPASMS ( 13 FDA reports)
SKIN EXFOLIATION ( 13 FDA reports)
THROMBOCYTOPENIA ( 13 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 13 FDA reports)
ABDOMINAL DISCOMFORT ( 12 FDA reports)
BACK PAIN ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
DRUG ERUPTION ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 11 FDA reports)
COMPLETED SUICIDE ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
HYPOKALAEMIA ( 11 FDA reports)
NEPHROTIC SYNDROME ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
BLISTER ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
HYPOAESTHESIA ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 10 FDA reports)
TREMOR ( 10 FDA reports)
URTICARIA ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
RHABDOMYOLYSIS ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
NERVOUSNESS ( 8 FDA reports)
ORAL PAIN ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
WOUND ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CEREBRAL ISCHAEMIA ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
EATING DISORDER ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HYPOVOLAEMIC SHOCK ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PULMONARY FIBROSIS ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SKIN BURNING SENSATION ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
ABDOMINAL MASS ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
BLOOD CALCIUM INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
GLOSSODYNIA ( 6 FDA reports)
GRAM STAIN ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 6 FDA reports)
TROPONIN INCREASED ( 6 FDA reports)
URINE COLOUR ABNORMAL ( 6 FDA reports)
AGEUSIA ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
APATHY ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ASCITES ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
CARDIAC FAILURE ACUTE ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 5 FDA reports)
FEELING DRUNK ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
MACULAR DEGENERATION ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PERSONALITY CHANGE ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
ARTERIAL REPAIR ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COMA ( 4 FDA reports)
CRYING ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GINGIVAL HYPERPLASIA ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HALLUCINATIONS, MIXED ( 4 FDA reports)
HOSTILITY ( 4 FDA reports)
IMPAIRED DRIVING ABILITY ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 4 FDA reports)
PROCTITIS ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANGER ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CAUSTIC INJURY ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
HAEMATOSPERMIA ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LUNG CYST ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
URETHRAL STENOSIS ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALIGNANT HYPERTENSION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS NONINFECTIVE ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NODULE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SCHAMBERG'S DISEASE ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ODOUR ABNORMAL ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
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ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
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ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
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BLADDER DISORDER ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
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BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
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BONE MARROW TOXICITY ( 1 FDA reports)
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BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
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BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
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CARDIAC MURMUR ( 1 FDA reports)
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CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
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COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
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CREPITATIONS ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
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CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
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ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
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ENTEROCOLITIS ( 1 FDA reports)
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FLUID INTAKE REDUCED ( 1 FDA reports)
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GASTRIC NEOPLASM ( 1 FDA reports)
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GASTROENTERITIS ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
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GOUT ( 1 FDA reports)
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HALLUCINATION, VISUAL ( 1 FDA reports)
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