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

DRUG INEFFECTIVE ( 50 FDA reports)
NAUSEA ( 44 FDA reports)
DIZZINESS ( 41 FDA reports)
HYPERTENSION ( 29 FDA reports)
DYSPNOEA ( 28 FDA reports)
HEADACHE ( 28 FDA reports)
BLOOD PRESSURE INCREASED ( 27 FDA reports)
DIARRHOEA ( 27 FDA reports)
INSOMNIA ( 26 FDA reports)
MYOCARDIAL INFARCTION ( 26 FDA reports)
ARTHRALGIA ( 25 FDA reports)
FATIGUE ( 24 FDA reports)
ASTHENIA ( 23 FDA reports)
HYPOTENSION ( 23 FDA reports)
VOMITING ( 23 FDA reports)
FALL ( 22 FDA reports)
OEDEMA PERIPHERAL ( 20 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 20 FDA reports)
HYPERSENSITIVITY ( 19 FDA reports)
WEIGHT DECREASED ( 19 FDA reports)
CEREBROVASCULAR ACCIDENT ( 18 FDA reports)
PYREXIA ( 18 FDA reports)
CHEST PAIN ( 17 FDA reports)
FEELING ABNORMAL ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
MALAISE ( 16 FDA reports)
MYALGIA ( 16 FDA reports)
PAIN ( 16 FDA reports)
SOMNOLENCE ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
RASH ( 15 FDA reports)
SYNCOPE ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
ASTHMA ( 14 FDA reports)
BACK PAIN ( 14 FDA reports)
AGITATION ( 13 FDA reports)
CONVULSION ( 13 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
HYPERHIDROSIS ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
PRODUCT QUALITY ISSUE ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 12 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
LUNG INFECTION ( 12 FDA reports)
RENAL FAILURE ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
DEHYDRATION ( 11 FDA reports)
DEPRESSION ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
RHINORRHOEA ( 11 FDA reports)
ANXIETY ( 10 FDA reports)
CATARACT ( 10 FDA reports)
CHEST DISCOMFORT ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
TREMOR ( 10 FDA reports)
CONTUSION ( 9 FDA reports)
COUGH ( 9 FDA reports)
DEATH ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
LARYNGITIS ( 9 FDA reports)
MUSCLE SPASMS ( 9 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
VISUAL ACUITY REDUCED ( 9 FDA reports)
CEREBELLAR SYNDROME ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
HIP FRACTURE ( 8 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
TINNITUS ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
RESTLESS LEGS SYNDROME ( 7 FDA reports)
SPINAL COLUMN INJURY ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEAD INJURY ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SWELLING ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
ULCER ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CHOLECYSTECTOMY ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
FACIAL BONES FRACTURE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MONOPLEGIA ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 4 FDA reports)
CEREBRAL ARTERY STENOSIS ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INFECTION ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LOWER LIMB DEFORMITY ( 4 FDA reports)
MOYAMOYA DISEASE ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 3 FDA reports)
APPETITE DISORDER ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BLADDER TELANGIECTASIA ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEAT STROKE ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SHOCK ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BLADDER CANCER STAGE II ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN STEM STROKE ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMANGIOMA CONGENITAL ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIPOMA EXCISION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUPUS VASCULITIS ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NIGHT CRAMPS ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE NORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER STAGE I ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHORIOCARCINOMA ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHOROIDAL HAEMORRHAGE ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NATURAL KILLER-CELL LEUKAEMIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF PRESSURE IN EAR ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WOUND ( 1 FDA reports)

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