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

DRUG INTERACTION ( 90 FDA reports)
FALL ( 83 FDA reports)
RENAL FAILURE ACUTE ( 70 FDA reports)
DYSPNOEA ( 63 FDA reports)
PYREXIA ( 63 FDA reports)
NAUSEA ( 61 FDA reports)
SOMNOLENCE ( 55 FDA reports)
PAIN ( 54 FDA reports)
VOMITING ( 53 FDA reports)
CONFUSIONAL STATE ( 51 FDA reports)
ANAEMIA ( 49 FDA reports)
SUICIDE ATTEMPT ( 48 FDA reports)
HEADACHE ( 43 FDA reports)
LOSS OF CONSCIOUSNESS ( 43 FDA reports)
OVERDOSE ( 42 FDA reports)
ABNORMAL BEHAVIOUR ( 41 FDA reports)
MALAISE ( 41 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 41 FDA reports)
ASTHENIA ( 36 FDA reports)
DIZZINESS ( 36 FDA reports)
RHABDOMYOLYSIS ( 36 FDA reports)
COMA ( 34 FDA reports)
HYPONATRAEMIA ( 33 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 31 FDA reports)
RENAL FAILURE ( 31 FDA reports)
BACK PAIN ( 29 FDA reports)
TRANSAMINASES INCREASED ( 29 FDA reports)
AGITATION ( 28 FDA reports)
AGRANULOCYTOSIS ( 28 FDA reports)
FATIGUE ( 28 FDA reports)
TREMOR ( 28 FDA reports)
DEPRESSION ( 27 FDA reports)
SYNCOPE ( 27 FDA reports)
THROMBOCYTOPENIA ( 27 FDA reports)
ANXIETY ( 26 FDA reports)
CYTOLYTIC HEPATITIS ( 26 FDA reports)
HYPOKALAEMIA ( 26 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 24 FDA reports)
CHEST PAIN ( 24 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 24 FDA reports)
HYPERTENSION ( 24 FDA reports)
ABDOMINAL PAIN ( 23 FDA reports)
COMPLETED SUICIDE ( 23 FDA reports)
BRADYCARDIA ( 22 FDA reports)
CONVULSION ( 22 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 22 FDA reports)
DEPRESSED MOOD ( 22 FDA reports)
DISORIENTATION ( 22 FDA reports)
PRURITUS ( 22 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 22 FDA reports)
CONSTIPATION ( 21 FDA reports)
CONDITION AGGRAVATED ( 20 FDA reports)
HYPOGLYCAEMIA ( 20 FDA reports)
HYPOTENSION ( 20 FDA reports)
SWELLING ( 20 FDA reports)
WEIGHT INCREASED ( 20 FDA reports)
COMPULSIVE SHOPPING ( 19 FDA reports)
DEHYDRATION ( 19 FDA reports)
MUSCLE RIGIDITY ( 19 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 19 FDA reports)
AKINESIA ( 18 FDA reports)
BALANCE DISORDER ( 18 FDA reports)
DRUG INEFFECTIVE ( 18 FDA reports)
HAEMATOMA ( 18 FDA reports)
MULTI-ORGAN FAILURE ( 18 FDA reports)
MYOCLONUS ( 18 FDA reports)
URINARY RETENTION ( 18 FDA reports)
VERTIGO ( 18 FDA reports)
DEATH ( 17 FDA reports)
DYSTHYMIC DISORDER ( 17 FDA reports)
HALLUCINATION ( 17 FDA reports)
IRRITABILITY ( 17 FDA reports)
LIVER INJURY ( 17 FDA reports)
MUSCULOSKELETAL PAIN ( 17 FDA reports)
SUICIDAL IDEATION ( 17 FDA reports)
ATRIAL FIBRILLATION ( 16 FDA reports)
CHROMATURIA ( 16 FDA reports)
CORNEAL REFLEX DECREASED ( 16 FDA reports)
DYSKINESIA ( 16 FDA reports)
HYPOMANIA ( 16 FDA reports)
NECK PAIN ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
PSYCHOTIC BEHAVIOUR ( 16 FDA reports)
RESPIRATORY ACIDOSIS ( 16 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
INJURY ( 15 FDA reports)
MUSCLE SPASMS ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
RASH ( 15 FDA reports)
WITHDRAWAL SYNDROME ( 15 FDA reports)
ABDOMINAL PAIN UPPER ( 14 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 14 FDA reports)
ARTHRALGIA ( 14 FDA reports)
CARDIAC ARREST ( 14 FDA reports)
DEEP VEIN THROMBOSIS ( 14 FDA reports)
INSOMNIA ( 14 FDA reports)
LEUKOPENIA ( 14 FDA reports)
MIOSIS ( 14 FDA reports)
RASH MACULO-PAPULAR ( 14 FDA reports)
TACHYCARDIA ( 14 FDA reports)
URINARY TRACT INFECTION ( 14 FDA reports)
AMIMIA ( 13 FDA reports)
CHOLESTASIS ( 13 FDA reports)
HEPATITIS ( 13 FDA reports)
HYPERGLYCAEMIA ( 13 FDA reports)
LUNG DISORDER ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
ARRHYTHMIA ( 12 FDA reports)
HEART RATE INCREASED ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
OEDEMA ( 12 FDA reports)
OFF LABEL USE ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
THROMBOSIS ( 12 FDA reports)
THYMUS DISORDER ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
CHOLECYSTITIS ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
DRUG DEPENDENCE ( 11 FDA reports)
DRUG LEVEL INCREASED ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
OSTEONECROSIS OF JAW ( 11 FDA reports)
SEROTONIN SYNDROME ( 11 FDA reports)
SKIN NECROSIS ( 11 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
GALLBLADDER DISORDER ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HYPOTHERMIA ( 10 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 10 FDA reports)
ILL-DEFINED DISORDER ( 10 FDA reports)
MEMORY IMPAIRMENT ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
SENSORY DISTURBANCE ( 10 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
BRADYPNOEA ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
COUGH ( 9 FDA reports)
DECREASED ACTIVITY ( 9 FDA reports)
DELIRIUM ( 9 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 9 FDA reports)
DISTURBANCE IN ATTENTION ( 9 FDA reports)
GASTRIC HAEMORRHAGE ( 9 FDA reports)
HALLUCINATION, VISUAL ( 9 FDA reports)
INFECTION ( 9 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
METASTASES TO LUNG ( 9 FDA reports)
NERVE COMPRESSION ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
ORAL INFECTION ( 9 FDA reports)
ORAL NEOPLASM ( 9 FDA reports)
OSTEITIS ( 9 FDA reports)
OSTEOARTHRITIS ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 9 FDA reports)
PURULENT DISCHARGE ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
UNEVALUABLE EVENT ( 9 FDA reports)
ABORTION SPONTANEOUS ( 8 FDA reports)
ATELECTASIS ( 8 FDA reports)
DERMATITIS BULLOUS ( 8 FDA reports)
DIPLOPIA ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
EXOSTOSIS ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
HEPATITIS ACUTE ( 8 FDA reports)
INCOHERENT ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
PATHOLOGICAL FRACTURE ( 8 FDA reports)
PREGNANCY ( 8 FDA reports)
QUADRIPARESIS ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
RHEUMATOID ARTHRITIS ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SKIN GRAFT FAILURE ( 8 FDA reports)
VISUAL IMPAIRMENT ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BRADYPHRENIA ( 7 FDA reports)
CEREBELLAR SYNDROME ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HEPATOCELLULAR INJURY ( 7 FDA reports)
INTENTIONAL DRUG MISUSE ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
METASTASES TO BONE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
NEURALGIA ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PARALYSIS ( 7 FDA reports)
PEMPHIGOID ( 7 FDA reports)
PETECHIAE ( 7 FDA reports)
POISONING DELIBERATE ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
ANOSOGNOSIA ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
CYST ( 6 FDA reports)
DELUSION ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
FLIGHT OF IDEAS ( 6 FDA reports)
FLUID RETENTION ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HEPATIC ENCEPHALOPATHY ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
MYDRIASIS ( 6 FDA reports)
NEUROSIS ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PURPURA ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SUSPICIOUSNESS ( 6 FDA reports)
TACHYPNOEA ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CHOLECYSTITIS CHRONIC ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
LEGIONELLA INFECTION ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
PAIN IN JAW ( 5 FDA reports)
PANCREATIC CARCINOMA ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PATHOLOGICAL GAMBLING ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
POLYARTHRITIS ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH PAPULAR ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
THEFT ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CHILLS ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DRUG ABUSE ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
HAEMARTHROSIS ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MONOPLEGIA ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
RASH MORBILLIFORM ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
SYNOVIAL CYST ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
CONJUNCTIVAL OEDEMA ( 3 FDA reports)
CRANIOTOMY ( 3 FDA reports)
DEBRIDEMENT ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EMOTIONAL POVERTY ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MIXED LIVER INJURY ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROSTATIC OBSTRUCTION ( 3 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PYELOCALIECTASIS ( 3 FDA reports)
PYOMYOSITIS ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RASH PAPULOSQUAMOUS ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SYMBLEPHARON ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
ULCER ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANION GAP DECREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTIC THROMBOSIS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLONIC OBSTRUCTION ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DROP ATTACKS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMMUNOLOGY TEST ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LYMPHADENITIS VIRAL ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
ON AND OFF PHENOMENON ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POISONING ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STATUS MIGRAINOSUS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
URETHRAL DISORDER ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VASCULAR NEOPLASM ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANGIOMYOLIPOMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BILE DUCT CANCER NON-RESECTABLE ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL DYSPLASIA ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL NEURALGIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHAGIC TUMOUR NECROSIS ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELECTIVE IGA IMMUNODEFICIENCY ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE I ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTIS CANCER ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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