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

CARDIAC ARREST ( 15 FDA reports)
PYREXIA ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
RASH ( 11 FDA reports)
RENAL FAILURE ACUTE ( 11 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
FALL ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
CHEST PAIN ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
DEATH ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
MALAISE ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
PAIN ( 6 FDA reports)
PULMONARY FIBROSIS ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
INFECTION ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
TREMOR ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
VOMITING ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
COMA ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HERNIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
INJURY ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COLLAGEN DISORDER ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
INTESTINAL STENOSIS ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET AGGREGATION INHIBITION ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PYURIA ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHONIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTED INSECT BITE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
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MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
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MOUNTAIN SICKNESS ACUTE ( 1 FDA reports)
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MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
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NAIL BED TENDERNESS ( 1 FDA reports)
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PAIN OF SKIN ( 1 FDA reports)
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PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
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PELVIC FRACTURE ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
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POLYP ( 1 FDA reports)
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PORPHYRIA NON-ACUTE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
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PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
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PULMONARY RADIATION INJURY ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
REITER'S SYNDROME ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
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RENAL FAILURE CHRONIC ( 1 FDA reports)
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RENAL NECROSIS ( 1 FDA reports)
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RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
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SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
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SERUM FERRITIN DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
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SKIN PAPILLOMA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
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SUICIDAL IDEATION ( 1 FDA reports)
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SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
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SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
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TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
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THYROID NEOPLASM ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
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TOOTHACHE ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
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VERTEBRAL COLUMN MASS ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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