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

FALL ( 110 FDA reports)
DEPRESSION ( 63 FDA reports)
TREMOR ( 62 FDA reports)
DYSPNOEA ( 61 FDA reports)
SUICIDE ATTEMPT ( 61 FDA reports)
ABNORMAL BEHAVIOUR ( 58 FDA reports)
BALANCE DISORDER ( 58 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 57 FDA reports)
WEIGHT INCREASED ( 56 FDA reports)
BACK PAIN ( 55 FDA reports)
DEPRESSED MOOD ( 55 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 55 FDA reports)
SUICIDAL IDEATION ( 54 FDA reports)
AKINESIA ( 52 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 52 FDA reports)
COMPULSIVE SHOPPING ( 51 FDA reports)
HYPOMANIA ( 51 FDA reports)
MUSCLE RIGIDITY ( 51 FDA reports)
MUSCULOSKELETAL PAIN ( 51 FDA reports)
NECK PAIN ( 51 FDA reports)
CHROMATURIA ( 50 FDA reports)
CORNEAL REFLEX DECREASED ( 50 FDA reports)
PSYCHOTIC BEHAVIOUR ( 50 FDA reports)
AMIMIA ( 49 FDA reports)
MUSCLE SPASMS ( 48 FDA reports)
THYMUS DISORDER ( 48 FDA reports)
AGITATION ( 47 FDA reports)
PYREXIA ( 43 FDA reports)
RENAL FAILURE ACUTE ( 41 FDA reports)
CONFUSIONAL STATE ( 40 FDA reports)
DRUG INTERACTION ( 34 FDA reports)
DYSTHYMIC DISORDER ( 33 FDA reports)
HYPONATRAEMIA ( 33 FDA reports)
IRRITABILITY ( 33 FDA reports)
SOMNOLENCE ( 33 FDA reports)
ANAEMIA ( 31 FDA reports)
MALAISE ( 31 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 30 FDA reports)
AGRANULOCYTOSIS ( 27 FDA reports)
VOMITING ( 27 FDA reports)
RENAL FAILURE ( 26 FDA reports)
DIARRHOEA ( 24 FDA reports)
NEUROSIS ( 24 FDA reports)
ASTHENIA ( 22 FDA reports)
NEUTROPENIA ( 22 FDA reports)
THROMBOCYTOPENIA ( 20 FDA reports)
DISORIENTATION ( 19 FDA reports)
HYPOTENSION ( 19 FDA reports)
BONE MARROW FAILURE ( 18 FDA reports)
DEATH ( 18 FDA reports)
HAEMATOMA ( 18 FDA reports)
PULMONARY EMBOLISM ( 18 FDA reports)
CYTOLYTIC HEPATITIS ( 17 FDA reports)
DRUG INEFFECTIVE ( 17 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 17 FDA reports)
DIZZINESS ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
INFLAMMATION ( 15 FDA reports)
LOSS OF CONSCIOUSNESS ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 14 FDA reports)
CARDIOMEGALY ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
COMA ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
PORTAL HYPERTENSION ( 12 FDA reports)
RHABDOMYOLYSIS ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
ANXIETY ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DISTURBANCE IN ATTENTION ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 11 FDA reports)
MELAENA ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
ABDOMINAL WALL CYST ( 10 FDA reports)
BRADYCARDIA ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BRADYPHRENIA ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DYSKINESIA ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
MYOCLONUS ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
ORTHOSTATIC HYPOTENSION ( 9 FDA reports)
AGGRESSION ( 8 FDA reports)
ANOREXIA ( 8 FDA reports)
FAECALOMA ( 8 FDA reports)
FEELING DRUNK ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
LACTIC ACIDOSIS ( 8 FDA reports)
POLYNEUROPATHY ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 7 FDA reports)
PHLEBITIS ( 7 FDA reports)
PULMONARY ALVEOLAR MICROLITHIASIS ( 7 FDA reports)
PYELONEPHRITIS ( 7 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PURPURA ( 6 FDA reports)
SHOCK ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
VASCULAR PURPURA ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CHEILITIS ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LEUKOCYTOSIS ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PATHOLOGICAL GAMBLING ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACINETOBACTER INFECTION ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
CATHETER SEPSIS ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EYE ROLLING ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
MYOCARDIAL ISCHAEMIA ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PARALYSIS ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANAEMIA MEGALOBLASTIC ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
CERVIX DISORDER ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EYE IRRITATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HAEMARTHROSIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
PAIN ( 3 FDA reports)
PEMPHIGUS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADRENOMEGALY ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BREAST HAEMATOMA ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYST ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 2 FDA reports)
DOLICHOCOLON ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
FAECALITH ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENDELSON'S SYNDROME ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
SCAB ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE POLYNEUROPATHY ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATONIC SEIZURES ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE NEUROPATHY ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSGLOBULINAEMIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GLARE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MACULE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL MYELOGRAM ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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