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

FALL ( 123 FDA reports)
DRUG INTERACTION ( 101 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 97 FDA reports)
SUICIDE ATTEMPT ( 88 FDA reports)
DIZZINESS ( 81 FDA reports)
CONFUSIONAL STATE ( 78 FDA reports)
OVERDOSE ( 76 FDA reports)
DEPRESSION ( 75 FDA reports)
SOMNOLENCE ( 75 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 72 FDA reports)
NAUSEA ( 69 FDA reports)
PYREXIA ( 67 FDA reports)
TREMOR ( 66 FDA reports)
LOSS OF CONSCIOUSNESS ( 64 FDA reports)
INSOMNIA ( 63 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 62 FDA reports)
ANXIETY ( 61 FDA reports)
FATIGUE ( 60 FDA reports)
DYSPNOEA ( 58 FDA reports)
AGITATION ( 55 FDA reports)
WEIGHT INCREASED ( 54 FDA reports)
ASTHENIA ( 53 FDA reports)
DEHYDRATION ( 53 FDA reports)
MALAISE ( 52 FDA reports)
DELIRIUM ( 50 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 49 FDA reports)
HEADACHE ( 48 FDA reports)
WEIGHT DECREASED ( 48 FDA reports)
HYPONATRAEMIA ( 46 FDA reports)
SUICIDAL IDEATION ( 46 FDA reports)
DIABETES MELLITUS ( 44 FDA reports)
DRUG TOXICITY ( 44 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 44 FDA reports)
PNEUMONIA ( 43 FDA reports)
VOMITING ( 43 FDA reports)
ABDOMINAL PAIN ( 42 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 42 FDA reports)
HYPERTENSION ( 42 FDA reports)
RASH ( 42 FDA reports)
CONVULSION ( 39 FDA reports)
DISORIENTATION ( 39 FDA reports)
TACHYCARDIA ( 39 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 38 FDA reports)
COMA ( 38 FDA reports)
ANAEMIA ( 37 FDA reports)
DIARRHOEA ( 37 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 37 FDA reports)
HYPOTENSION ( 37 FDA reports)
PLEURAL EFFUSION ( 37 FDA reports)
URINARY RETENTION ( 37 FDA reports)
CYTOLYTIC HEPATITIS ( 36 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 35 FDA reports)
DRUG INEFFECTIVE ( 35 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 35 FDA reports)
AGGRESSION ( 34 FDA reports)
RESTLESSNESS ( 34 FDA reports)
HYPERHIDROSIS ( 33 FDA reports)
PAIN ( 33 FDA reports)
RENAL FAILURE ACUTE ( 33 FDA reports)
CONSTIPATION ( 31 FDA reports)
OEDEMA PERIPHERAL ( 31 FDA reports)
ORTHOSTATIC HYPOTENSION ( 31 FDA reports)
PREMATURE BABY ( 31 FDA reports)
RENAL FAILURE ( 31 FDA reports)
TOXIC SKIN ERUPTION ( 31 FDA reports)
PRURITUS ( 30 FDA reports)
CHOLESTASIS ( 29 FDA reports)
CONDITION AGGRAVATED ( 29 FDA reports)
HEPATIC ENZYME INCREASED ( 29 FDA reports)
OFF LABEL USE ( 29 FDA reports)
SEROTONIN SYNDROME ( 29 FDA reports)
RHABDOMYOLYSIS ( 28 FDA reports)
DECREASED APPETITE ( 27 FDA reports)
ABNORMAL BEHAVIOUR ( 26 FDA reports)
HYPOKALAEMIA ( 26 FDA reports)
MULTIPLE DRUG OVERDOSE ( 26 FDA reports)
PULMONARY EMBOLISM ( 26 FDA reports)
GAIT DISTURBANCE ( 25 FDA reports)
ROAD TRAFFIC ACCIDENT ( 25 FDA reports)
CHEST PAIN ( 24 FDA reports)
EPILEPSY ( 24 FDA reports)
HALLUCINATION, VISUAL ( 24 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 24 FDA reports)
THROMBOCYTOPENIA ( 24 FDA reports)
URINARY TRACT INFECTION ( 24 FDA reports)
BLOOD CREATININE INCREASED ( 23 FDA reports)
BLOOD PRESSURE INCREASED ( 23 FDA reports)
TRANSAMINASES INCREASED ( 23 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 22 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 22 FDA reports)
HYPERGLYCAEMIA ( 22 FDA reports)
IRRITABILITY ( 22 FDA reports)
LUNG DISORDER ( 22 FDA reports)
VERTIGO ( 22 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 21 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 21 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
DYSPHAGIA ( 21 FDA reports)
HYPOAESTHESIA ( 21 FDA reports)
RESPIRATORY FAILURE ( 21 FDA reports)
STEVENS-JOHNSON SYNDROME ( 21 FDA reports)
SUBDURAL HAEMATOMA ( 21 FDA reports)
THROMBOSIS ( 21 FDA reports)
BACK PAIN ( 20 FDA reports)
HYPOGLYCAEMIA ( 20 FDA reports)
LEUKOPENIA ( 20 FDA reports)
ANURIA ( 19 FDA reports)
CHOLELITHIASIS ( 19 FDA reports)
COMPLETED SUICIDE ( 19 FDA reports)
DEATH ( 19 FDA reports)
DRUG LEVEL INCREASED ( 19 FDA reports)
ERYTHEMA ( 19 FDA reports)
HEART RATE INCREASED ( 19 FDA reports)
HEPATIC STEATOSIS ( 19 FDA reports)
ILEUS ( 19 FDA reports)
PARKINSONISM ( 19 FDA reports)
STATUS EPILEPTICUS ( 19 FDA reports)
ANOREXIA ( 18 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 18 FDA reports)
BLOOD UREA INCREASED ( 18 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 18 FDA reports)
INTENTIONAL OVERDOSE ( 18 FDA reports)
MANIA ( 18 FDA reports)
PULMONARY OEDEMA ( 18 FDA reports)
SEPTIC SHOCK ( 18 FDA reports)
SYNCOPE ( 18 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 18 FDA reports)
AMNESIA ( 17 FDA reports)
BLOOD GLUCOSE INCREASED ( 17 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 17 FDA reports)
CONTUSION ( 17 FDA reports)
HALLUCINATION ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
PSYCHOTIC DISORDER ( 17 FDA reports)
SPEECH DISORDER ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
CAESAREAN SECTION ( 16 FDA reports)
ERECTILE DYSFUNCTION ( 16 FDA reports)
HEPATIC FAILURE ( 16 FDA reports)
MYOCARDIAL INFARCTION ( 16 FDA reports)
PANIC ATTACK ( 16 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 16 FDA reports)
URTICARIA ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 16 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 15 FDA reports)
CARDIAC ARREST ( 15 FDA reports)
DIABETIC KETOACIDOSIS ( 15 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 15 FDA reports)
HEPATITIS ACUTE ( 15 FDA reports)
INTERSTITIAL LUNG DISEASE ( 15 FDA reports)
OBESITY ( 15 FDA reports)
OEDEMA ( 15 FDA reports)
OXYGEN SATURATION DECREASED ( 15 FDA reports)
PANCYTOPENIA ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
RESPIRATORY DISTRESS ( 15 FDA reports)
SOPOR ( 15 FDA reports)
ASCITES ( 14 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 14 FDA reports)
MUSCLE RIGIDITY ( 14 FDA reports)
PALPITATIONS ( 14 FDA reports)
PANCREATITIS ( 14 FDA reports)
BLOOD PRESSURE DECREASED ( 13 FDA reports)
BLOOD SODIUM DECREASED ( 13 FDA reports)
COGNITIVE DISORDER ( 13 FDA reports)
CRYING ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
DISTURBANCE IN ATTENTION ( 13 FDA reports)
DYSSTASIA ( 13 FDA reports)
DYSURIA ( 13 FDA reports)
HAEMOGLOBIN DECREASED ( 13 FDA reports)
HEAD INJURY ( 13 FDA reports)
HYPERTHERMIA ( 13 FDA reports)
INCREASED APPETITE ( 13 FDA reports)
INFLAMMATION ( 13 FDA reports)
JAUNDICE ( 13 FDA reports)
LEUKOCYTOSIS ( 13 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
OSTEONECROSIS ( 13 FDA reports)
PANCREATITIS ACUTE ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
ATRIAL SEPTAL DEFECT ( 12 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 12 FDA reports)
DYSKINESIA ( 12 FDA reports)
FEEDING DISORDER NEONATAL ( 12 FDA reports)
FEELING HOT ( 12 FDA reports)
HAEMATOMA ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
HYPOTONIA ( 12 FDA reports)
INTENTIONAL SELF-INJURY ( 12 FDA reports)
LYMPHADENOPATHY ( 12 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 12 FDA reports)
MYOCLONUS ( 12 FDA reports)
VISION BLURRED ( 12 FDA reports)
AGITATION NEONATAL ( 11 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
DRUG DEPENDENCE ( 11 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
HEPATITIS ( 11 FDA reports)
HEPATITIS CHOLESTATIC ( 11 FDA reports)
HYPERTONIA NEONATAL ( 11 FDA reports)
HYPOTONIA NEONATAL ( 11 FDA reports)
INCORRECT DOSE ADMINISTERED ( 11 FDA reports)
LABYRINTHITIS ( 11 FDA reports)
POLYHYDRAMNIOS ( 11 FDA reports)
PREGNANCY ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
STUPOR ( 11 FDA reports)
SUDDEN DEATH ( 11 FDA reports)
ABDOMINAL DISTENSION ( 10 FDA reports)
ABNORMAL DREAMS ( 10 FDA reports)
AGRANULOCYTOSIS ( 10 FDA reports)
ALCOHOLIC LIVER DISEASE ( 10 FDA reports)
CARDIAC DISORDER ( 10 FDA reports)
CARDIOMEGALY ( 10 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 10 FDA reports)
CYANOSIS NEONATAL ( 10 FDA reports)
DELUSION ( 10 FDA reports)
DIFFICULTY IN WALKING ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
EATING DISORDER ( 10 FDA reports)
EJECTION FRACTION DECREASED ( 10 FDA reports)
GRAND MAL CONVULSION ( 10 FDA reports)
HEPATITIS FULMINANT ( 10 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 10 FDA reports)
MAJOR DEPRESSION ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
NEONATAL TACHYPNOEA ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
SHOCK ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
VENTRICULAR TACHYCARDIA ( 10 FDA reports)
ACIDOSIS ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
BALANCE DISORDER ( 9 FDA reports)
BRADYCARDIA NEONATAL ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 9 FDA reports)
CHILLS ( 9 FDA reports)
DRUG ABUSE ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
HEART RATE DECREASED ( 9 FDA reports)
HYPOTHERMIA ( 9 FDA reports)
INFANTILE APNOEIC ATTACK ( 9 FDA reports)
INFECTION ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
MEMORY IMPAIRMENT ( 9 FDA reports)
MYDRIASIS ( 9 FDA reports)
NEONATAL DISORDER ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
NEUTROPHIL COUNT INCREASED ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
SEDATION ( 9 FDA reports)
SLEEP APNOEA SYNDROME ( 9 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 9 FDA reports)
TREMOR NEONATAL ( 9 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 8 FDA reports)
BONE PAIN ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
CIRCULATORY COLLAPSE ( 8 FDA reports)
COUGH ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
EJACULATION FAILURE ( 8 FDA reports)
FEMUR FRACTURE ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
HYPERLIPIDAEMIA ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
HYPERTONIA ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
INTENTIONAL MISUSE ( 8 FDA reports)
LIVER INJURY ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
RASH MACULO-PAPULAR ( 8 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 8 FDA reports)
STRIDOR ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
TYPE 2 DIABETES MELLITUS ( 8 FDA reports)
VENOUS THROMBOSIS ( 8 FDA reports)
ABULIA ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
CEREBRAL ATROPHY ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
COLD SWEAT ( 7 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 7 FDA reports)
CONVULSION NEONATAL ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CYANOSIS ( 7 FDA reports)
DEVELOPMENTAL DELAY ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
FEAR ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HEPATIC CIRRHOSIS ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
ILEUS PARALYTIC ( 7 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
NEURALGIA ( 7 FDA reports)
NIGHTMARE ( 7 FDA reports)
PHONOLOGICAL DISORDER ( 7 FDA reports)
PURPURA ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
SALIVARY HYPERSECRETION ( 7 FDA reports)
SMALL FOR DATES BABY ( 7 FDA reports)
SOMATIC DELUSION ( 7 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
URINARY INCONTINENCE ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
ABNORMAL FAECES ( 6 FDA reports)
ACQUIRED EPILEPTIC APHASIA ( 6 FDA reports)
AKATHISIA ( 6 FDA reports)
ALCOHOLISM ( 6 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
APGAR SCORE LOW ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
AUTISM ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
CARDIOMYOPATHY ( 6 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DIABETIC NEUROPATHY ( 6 FDA reports)
DRUG ABUSER ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DRY SKIN ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GASTRIC DISORDER ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
HAEMORRHOIDS ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HYPERAMMONAEMIA ( 6 FDA reports)
HYPERNATRAEMIA ( 6 FDA reports)
INJURY ( 6 FDA reports)
LACTOSE INTOLERANCE ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
MENTAL IMPAIRMENT ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OESOPHAGITIS ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PULMONARY CONGESTION ( 6 FDA reports)
QRS AXIS ABNORMAL ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 6 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 6 FDA reports)
TACHYPNOEA ( 6 FDA reports)
TREATMENT NONCOMPLIANCE ( 6 FDA reports)
UMBILICAL CORD PROLAPSE ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
WOUND DEBRIDEMENT ( 6 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 5 FDA reports)
BLOOD CORTISOL INCREASED ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD PROLACTIN INCREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 5 FDA reports)
CHILD ABUSE ( 5 FDA reports)
CHOLESTEROL GRANULOMA ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
COLITIS MICROSCOPIC ( 5 FDA reports)
DEVICE FAILURE ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
ECCHYMOSIS ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FEVER NEONATAL ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HEPATOCELLULAR INJURY ( 5 FDA reports)
HEPATOSPLENOMEGALY ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
IMPAIRED DRIVING ABILITY ( 5 FDA reports)
IMPULSIVE BEHAVIOUR ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LARYNGEAL DISORDER ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LOWER LIMB FRACTURE ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
NEOPLASM ( 5 FDA reports)
OPISTHOTONUS ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
OSTEITIS ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PANCREATIC PSEUDOCYST ( 5 FDA reports)
PERONEAL NERVE PALSY ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PSYCHIATRIC SYMPTOM ( 5 FDA reports)
RENAL APLASIA ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
RETROPERITONEAL FIBROSIS ( 5 FDA reports)
SCIATICA ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SOMNOLENCE NEONATAL ( 5 FDA reports)
STRESS ( 5 FDA reports)
SURGERY ( 5 FDA reports)
SWELLING ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TARDIVE DYSKINESIA ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VOCAL CORD PARALYSIS ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ACCIDENT ( 4 FDA reports)
ANORECTAL DISORDER ( 4 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
APATHY ( 4 FDA reports)
APLASIA ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BLOOD ALCOHOL INCREASED ( 4 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
BREAST CANCER RECURRENT ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
EXCITABILITY ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
FEEDING PROBLEM IN NEWBORN ( 4 FDA reports)
FIBROMYALGIA ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GLOSSOPTOSIS ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPORESPONSIVE TO STIMULI ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTERCOSTAL RETRACTION ( 4 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
JOINT SPRAIN ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
MICROGNATHIA ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
NEONATAL APNOEIC ATTACK ( 4 FDA reports)
NEONATAL TACHYCARDIA ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
POOR SUCKING REFLEX ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RENAL COLIC ( 4 FDA reports)
RENIN INCREASED ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
THIRST ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
APNOEA ( 3 FDA reports)
APPENDICECTOMY ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
CARDIAC FIBRILLATION ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHOREA ( 3 FDA reports)
CLONUS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 3 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 3 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
FACTOR X DEFICIENCY ( 3 FDA reports)
FAECAL INCONTINENCE ( 3 FDA reports)
FANCONI SYNDROME ACQUIRED ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FOETAL CARDIAC DISORDER ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
FUMBLING ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEREDITARY ANGIOEDEMA ( 3 FDA reports)
HIGH ARCHED PALATE ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
JAUNDICE NEONATAL ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LICHENIFICATION ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MASS ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEONATAL ASPHYXIA ( 3 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEURODERMATITIS ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHIMOSIS ( 3 FDA reports)
PLACENTAL DISORDER ( 3 FDA reports)
PLACENTAL INFARCTION ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RADIATION MUCOSITIS ( 3 FDA reports)
REGURGITATION ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
RETROGNATHIA ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STARING ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
TENSION ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
ULCER ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACETONAEMIA ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMIMIA ( 2 FDA reports)
AMYOTROPHY ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ARTIFICIAL MENOPAUSE ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BALLISMUS ( 2 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BONE DEBRIDEMENT ( 2 FDA reports)
BONE DENSITY ABNORMAL ( 2 FDA reports)
BORRELIA INFECTION ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BULLOUS LUNG DISEASE ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHOROIDAL DETACHMENT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COARCTATION OF THE AORTA ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLEX PARTIAL SEIZURES ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL LIMB HYPEREXTENSION ( 2 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 2 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMO-HYPODERMITIS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCONVULSIVE THERAPY ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FIXED ERUPTION ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOETAL VALPROATE SYNDROME ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GENERAL ANAESTHESIA ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HIP DYSPLASIA ( 2 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERCHROMASIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LARYNGOMALACIA ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEONATAL HEPATOMEGALY ( 2 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NODULE ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
ORAL CAVITY FISTULA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL EROSION ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PIERRE ROBIN SYNDROME ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLASTIC SURGERY ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYARTHRITIS ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL CANCER STAGE III ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 2 FDA reports)
RETROGRADE EJACULATION ( 2 FDA reports)
SCAR ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SIGNET-RING CELL CARCINOMA ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VAGINITIS GARDNERELLA ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WEIGHT GAIN POOR ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTI-HBS ANTIBODY ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-B ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC ARREST NEONATAL ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIOMYOPATHY ACUTE ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
CATARACT NUCLEAR ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
CONGENITAL CEREBRAL CYST ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL TERATOMA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEAR OF WEIGHT GAIN ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FOETAL ARRHYTHMIA ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOETAL HEART RATE DISORDER ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ANXIETY DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HABITUAL ABORTION ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HALLUCINATION, GUSTATORY ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEREDITARY ATAXIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPETIGO ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MURDER ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCTIPHOBIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OVARIAN ADHESION ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PELVIC ADHESIONS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PHYSIOTHERAPY ( 1 FDA reports)
PLACENTA PRAEVIA HAEMORRHAGE ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYTRAUMATISM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREAURICULAR CYST ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYROMANIA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
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RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RETROPERITONEAL EFFUSION ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIB DEFORMITY ( 1 FDA reports)
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SALIVARY GLAND DISORDER ( 1 FDA reports)
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SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
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SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
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SMALL CELL CARCINOMA ( 1 FDA reports)
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SPIDER VEIN ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
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STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
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TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
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TRYPTASE INCREASED ( 1 FDA reports)
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TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
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