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

NEUROLEPTIC MALIGNANT SYNDROME ( 173 FDA reports)
PYREXIA ( 158 FDA reports)
DRUG INTERACTION ( 150 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 129 FDA reports)
SOMNOLENCE ( 111 FDA reports)
DELIRIUM ( 107 FDA reports)
FALL ( 105 FDA reports)
TREMOR ( 105 FDA reports)
SUICIDE ATTEMPT ( 103 FDA reports)
PNEUMONIA ( 100 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 90 FDA reports)
INSOMNIA ( 90 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 87 FDA reports)
AGITATION ( 82 FDA reports)
RESTLESSNESS ( 80 FDA reports)
VOMITING ( 80 FDA reports)
OVERDOSE ( 79 FDA reports)
SCHIZOPHRENIA ( 78 FDA reports)
HALLUCINATION ( 77 FDA reports)
DIZZINESS ( 76 FDA reports)
TACHYCARDIA ( 76 FDA reports)
CONFUSIONAL STATE ( 75 FDA reports)
CONVULSION ( 74 FDA reports)
RHABDOMYOLYSIS ( 73 FDA reports)
COMA ( 72 FDA reports)
DYSPNOEA ( 71 FDA reports)
LOSS OF CONSCIOUSNESS ( 67 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 66 FDA reports)
HYPONATRAEMIA ( 64 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 63 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 62 FDA reports)
CONDITION AGGRAVATED ( 61 FDA reports)
DEPRESSION ( 61 FDA reports)
DISORIENTATION ( 60 FDA reports)
AGGRESSION ( 59 FDA reports)
NAUSEA ( 59 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 58 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 57 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 57 FDA reports)
CONSTIPATION ( 56 FDA reports)
DRUG INEFFECTIVE ( 55 FDA reports)
ABNORMAL BEHAVIOUR ( 54 FDA reports)
GAIT DISTURBANCE ( 52 FDA reports)
WEIGHT INCREASED ( 52 FDA reports)
CARDIO-RESPIRATORY ARREST ( 50 FDA reports)
COMPLETED SUICIDE ( 50 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 50 FDA reports)
MALAISE ( 50 FDA reports)
RENAL FAILURE ACUTE ( 50 FDA reports)
BLOOD GLUCOSE INCREASED ( 49 FDA reports)
PARKINSONISM ( 49 FDA reports)
FATIGUE ( 48 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 48 FDA reports)
THROMBOCYTOPENIA ( 48 FDA reports)
CARDIAC ARREST ( 47 FDA reports)
HYPERHIDROSIS ( 47 FDA reports)
AKATHISIA ( 46 FDA reports)
IRRITABILITY ( 46 FDA reports)
ASTHENIA ( 45 FDA reports)
DIARRHOEA ( 45 FDA reports)
HALLUCINATION, AUDITORY ( 45 FDA reports)
URINARY RETENTION ( 45 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 45 FDA reports)
ANXIETY ( 44 FDA reports)
PULMONARY EMBOLISM ( 44 FDA reports)
CARDIAC FAILURE ( 43 FDA reports)
HYPERTENSION ( 43 FDA reports)
SUICIDAL IDEATION ( 42 FDA reports)
DYSKINESIA ( 41 FDA reports)
LIVER DISORDER ( 41 FDA reports)
DYSPHAGIA ( 39 FDA reports)
DEATH ( 38 FDA reports)
ILEUS ( 38 FDA reports)
PSYCHOTIC DISORDER ( 38 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 37 FDA reports)
DELUSION ( 37 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 37 FDA reports)
LEUKOPENIA ( 37 FDA reports)
RASH ( 37 FDA reports)
HYPOTENSION ( 36 FDA reports)
SEDATION ( 36 FDA reports)
SEPSIS ( 36 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 35 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 34 FDA reports)
MYDRIASIS ( 34 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 34 FDA reports)
SUDDEN DEATH ( 34 FDA reports)
MUSCLE RIGIDITY ( 33 FDA reports)
ANAEMIA ( 32 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 32 FDA reports)
BLOOD CREATININE INCREASED ( 31 FDA reports)
CEREBRAL INFARCTION ( 31 FDA reports)
DEHYDRATION ( 31 FDA reports)
RENAL FAILURE ( 31 FDA reports)
DECREASED APPETITE ( 30 FDA reports)
INTENTIONAL OVERDOSE ( 30 FDA reports)
RESPIRATORY FAILURE ( 30 FDA reports)
COGNITIVE DISORDER ( 29 FDA reports)
COUGH ( 29 FDA reports)
FEELING ABNORMAL ( 29 FDA reports)
HYPOAESTHESIA ( 29 FDA reports)
PLATELET COUNT DECREASED ( 29 FDA reports)
PNEUMONIA ASPIRATION ( 29 FDA reports)
DRUG TOXICITY ( 28 FDA reports)
OEDEMA PERIPHERAL ( 28 FDA reports)
SPEECH DISORDER ( 28 FDA reports)
WEIGHT DECREASED ( 28 FDA reports)
HAEMOGLOBIN DECREASED ( 26 FDA reports)
SLEEP DISORDER ( 26 FDA reports)
SYNCOPE ( 26 FDA reports)
HEADACHE ( 25 FDA reports)
HEART RATE INCREASED ( 25 FDA reports)
SALIVARY HYPERSECRETION ( 25 FDA reports)
AGRANULOCYTOSIS ( 24 FDA reports)
ARRHYTHMIA ( 24 FDA reports)
BLOOD PRESSURE INCREASED ( 24 FDA reports)
DYSTONIA ( 24 FDA reports)
HALLUCINATION, VISUAL ( 24 FDA reports)
HYPOGLYCAEMIA ( 24 FDA reports)
HYPOKALAEMIA ( 24 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 24 FDA reports)
PLEURAL EFFUSION ( 24 FDA reports)
THIRST ( 24 FDA reports)
ABDOMINAL PAIN ( 23 FDA reports)
BRADYCARDIA ( 23 FDA reports)
DIABETES MELLITUS ( 23 FDA reports)
EOSINOPHIL COUNT INCREASED ( 23 FDA reports)
MEMORY IMPAIRMENT ( 23 FDA reports)
NEUTROPENIA ( 23 FDA reports)
TREATMENT NONCOMPLIANCE ( 23 FDA reports)
EPILEPSY ( 22 FDA reports)
MULTIPLE DRUG OVERDOSE ( 22 FDA reports)
MYOCARDIAL INFARCTION ( 22 FDA reports)
SOPOR ( 22 FDA reports)
BLOOD UREA INCREASED ( 21 FDA reports)
CIRCULATORY COLLAPSE ( 21 FDA reports)
DRUG LEVEL INCREASED ( 21 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 21 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 21 FDA reports)
HEPATITIS ( 21 FDA reports)
HEPATITIS ACUTE ( 21 FDA reports)
MENTAL DISORDER ( 21 FDA reports)
OEDEMA ( 21 FDA reports)
STATUS EPILEPTICUS ( 21 FDA reports)
BACK PAIN ( 20 FDA reports)
CHILLS ( 20 FDA reports)
DRUG ERUPTION ( 20 FDA reports)
PAIN ( 20 FDA reports)
PARANOIA ( 20 FDA reports)
ABASIA ( 19 FDA reports)
APALLIC SYNDROME ( 19 FDA reports)
ATRIAL FIBRILLATION ( 19 FDA reports)
CATATONIA ( 19 FDA reports)
DEPRESSIVE SYMPTOM ( 19 FDA reports)
GRAND MAL CONVULSION ( 19 FDA reports)
HEAD INJURY ( 19 FDA reports)
HYPOTHERMIA ( 19 FDA reports)
LEUKOCYTOSIS ( 19 FDA reports)
PULMONARY OEDEMA ( 19 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 18 FDA reports)
BLOOD PROLACTIN INCREASED ( 18 FDA reports)
ERYTHEMA ( 18 FDA reports)
HAEMATOCRIT DECREASED ( 18 FDA reports)
NERVOUSNESS ( 18 FDA reports)
PERSECUTORY DELUSION ( 18 FDA reports)
POLLAKIURIA ( 18 FDA reports)
PRURITUS ( 18 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 17 FDA reports)
DYSARTHRIA ( 17 FDA reports)
HYPERKALAEMIA ( 17 FDA reports)
HYPOXIA ( 17 FDA reports)
INFECTION ( 17 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 17 FDA reports)
RESPIRATORY ARREST ( 17 FDA reports)
URINARY TRACT INFECTION ( 17 FDA reports)
ACUTE HEPATIC FAILURE ( 16 FDA reports)
BODY TEMPERATURE INCREASED ( 16 FDA reports)
EPISTAXIS ( 16 FDA reports)
GALLBLADDER OEDEMA ( 16 FDA reports)
MUSCLE SPASMS ( 16 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
ORTHOSTATIC HYPOTENSION ( 16 FDA reports)
PREGNANCY ( 16 FDA reports)
RENAL IMPAIRMENT ( 16 FDA reports)
SLUGGISHNESS ( 16 FDA reports)
VISUAL IMPAIRMENT ( 16 FDA reports)
BLOOD POTASSIUM DECREASED ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 15 FDA reports)
CARDIOMEGALY ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
SEROTONIN SYNDROME ( 15 FDA reports)
VERTIGO ( 15 FDA reports)
AMNESIA ( 14 FDA reports)
BALANCE DISORDER ( 14 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 14 FDA reports)
GASTROINTESTINAL DISORDER ( 14 FDA reports)
HAEMORRHAGE ( 14 FDA reports)
HYPERPROLACTINAEMIA ( 14 FDA reports)
NEUROGENIC BLADDER ( 14 FDA reports)
NEUTROPHIL COUNT INCREASED ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
RESPIRATORY DEPRESSION ( 14 FDA reports)
VENTRICULAR FIBRILLATION ( 14 FDA reports)
ANOREXIA ( 13 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
CLONIC CONVULSION ( 13 FDA reports)
DEPRESSED MOOD ( 13 FDA reports)
HYPERGLYCAEMIA ( 13 FDA reports)
ILEUS PARALYTIC ( 13 FDA reports)
INCORRECT DOSE ADMINISTERED ( 13 FDA reports)
MUTISM ( 13 FDA reports)
PROTEIN URINE PRESENT ( 13 FDA reports)
STEVENS-JOHNSON SYNDROME ( 13 FDA reports)
TRANSAMINASES INCREASED ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
ASCITES ( 12 FDA reports)
BEDRIDDEN ( 12 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 12 FDA reports)
DISTURBANCE IN ATTENTION ( 12 FDA reports)
DRY MOUTH ( 12 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
JAUNDICE ( 12 FDA reports)
OFF LABEL USE ( 12 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 12 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 12 FDA reports)
ABORTION SPONTANEOUS ( 11 FDA reports)
ASTHMA ( 11 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
BRADYKINESIA ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CHOLESTASIS ( 11 FDA reports)
CYANOSIS ( 11 FDA reports)
DRUG LEVEL DECREASED ( 11 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 11 FDA reports)
ELECTROLYTE IMBALANCE ( 11 FDA reports)
ENCEPHALOPATHY ( 11 FDA reports)
HYPERVENTILATION ( 11 FDA reports)
HYPOKINESIA ( 11 FDA reports)
INTRA-UTERINE DEATH ( 11 FDA reports)
LACTIC ACIDOSIS ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
MYOCARDITIS ( 11 FDA reports)
PLEUROTHOTONUS ( 11 FDA reports)
POLYDIPSIA ( 11 FDA reports)
POSTURE ABNORMAL ( 11 FDA reports)
TACHYPNOEA ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 11 FDA reports)
URINARY INCONTINENCE ( 11 FDA reports)
URINE OUTPUT DECREASED ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
ARTHRALGIA ( 10 FDA reports)
ASPHYXIA ( 10 FDA reports)
BRAIN OEDEMA ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
CHOKING ( 10 FDA reports)
COORDINATION ABNORMAL ( 10 FDA reports)
DERMATITIS ( 10 FDA reports)
DYSURIA ( 10 FDA reports)
EXCITABILITY ( 10 FDA reports)
GALACTORRHOEA ( 10 FDA reports)
GRANULOCYTE COUNT DECREASED ( 10 FDA reports)
HEPATIC ENZYME INCREASED ( 10 FDA reports)
HUNGER ( 10 FDA reports)
MANIA ( 10 FDA reports)
MOTOR DYSFUNCTION ( 10 FDA reports)
MUSCLE DISORDER ( 10 FDA reports)
MYOPATHY ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
PELVIC FRACTURE ( 10 FDA reports)
PLEURISY ( 10 FDA reports)
SENSORY DISTURBANCE ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
ABDOMINAL DISTENSION ( 9 FDA reports)
ANGER ( 9 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 9 FDA reports)
BRAIN DEATH ( 9 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 9 FDA reports)
GASTROINTESTINAL INJURY ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
HYPERPHAGIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
INFLAMMATION ( 9 FDA reports)
INFLUENZA ( 9 FDA reports)
LYMPHADENOPATHY ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
MENSTRUATION DELAYED ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
OROPHARYNGEAL SPASM ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PARALYSIS ( 9 FDA reports)
PLATELET COUNT INCREASED ( 9 FDA reports)
PNEUMOTHORAX ( 9 FDA reports)
PSYCHIATRIC SYMPTOM ( 9 FDA reports)
PULMONARY INFARCTION ( 9 FDA reports)
SPLENIC INJURY ( 9 FDA reports)
STUPOR ( 9 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 8 FDA reports)
APATHY ( 8 FDA reports)
APPENDICITIS ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
CARDIOPULMONARY FAILURE ( 8 FDA reports)
COLON INJURY ( 8 FDA reports)
CRYING ( 8 FDA reports)
CYTOLYTIC HEPATITIS ( 8 FDA reports)
DIET REFUSAL ( 8 FDA reports)
DIVERTICULITIS ( 8 FDA reports)
DROOLING ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
FINGER DEFORMITY ( 8 FDA reports)
GASTROINTESTINAL PERFORATION ( 8 FDA reports)
HOSPITALISATION ( 8 FDA reports)
HYPERTHERMIA ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INFECTIOUS PERITONITIS ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
INTENTIONAL SELF-INJURY ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
KETOACIDOSIS ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 8 FDA reports)
MOBILITY DECREASED ( 8 FDA reports)
MYOCLONUS ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
OCULOGYRIC CRISIS ( 8 FDA reports)
ORTHOSTATIC HYPERTENSION ( 8 FDA reports)
OVARIAN CYST ( 8 FDA reports)
PAROXYSMAL PERCEPTUAL ALTERATION ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 8 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
TALIPES ( 8 FDA reports)
TARDIVE DYSKINESIA ( 8 FDA reports)
TRAUMATIC LUNG INJURY ( 8 FDA reports)
UNRESPONSIVE TO STIMULI ( 8 FDA reports)
VAGINAL DISCHARGE ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ABORTION INDUCED ( 7 FDA reports)
ALCOHOLISM ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
ATAXIA ( 7 FDA reports)
ATELECTASIS ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD URINE PRESENT ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
CARDIAC PACEMAKER INSERTION ( 7 FDA reports)
COGWHEEL RIGIDITY ( 7 FDA reports)
CONDUCTION DISORDER ( 7 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 7 FDA reports)
DECUBITUS ULCER ( 7 FDA reports)
DEPENDENCE ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
FACE OEDEMA ( 7 FDA reports)
FEELING JITTERY ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
HELLP SYNDROME ( 7 FDA reports)
HYPERNATRAEMIA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPOAESTHESIA FACIAL ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
MENSTRUAL DISORDER ( 7 FDA reports)
MOVEMENT DISORDER ( 7 FDA reports)
MULTIPLE FRACTURES ( 7 FDA reports)
MUSCLE TIGHTNESS ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
NERVE INJURY ( 7 FDA reports)
NIGHTMARE ( 7 FDA reports)
OCULAR HYPERAEMIA ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PARKINSON'S DISEASE ( 7 FDA reports)
PERIARTHRITIS ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PULSE ABSENT ( 7 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 7 FDA reports)
SINUS TACHYCARDIA ( 7 FDA reports)
TENSION ( 7 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 7 FDA reports)
URINARY BLADDER RUPTURE ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
ANTICHOLINERGIC SYNDROME ( 6 FDA reports)
ASPERGILLOSIS ORAL ( 6 FDA reports)
BACTERIA URINE ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
DIABETES INSIPIDUS ( 6 FDA reports)
DIABETIC COMA ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FEAR ( 6 FDA reports)
FRACTURE ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HAEMODYNAMIC INSTABILITY ( 6 FDA reports)
HEPATITIS TOXIC ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
INCONTINENCE ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MENTAL IMPAIRMENT ( 6 FDA reports)
MICTURITION DISORDER ( 6 FDA reports)
MIOSIS ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
NODULE ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
PULMONARY CONGESTION ( 6 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 6 FDA reports)
REFLUX OESOPHAGITIS ( 6 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SOLILOQUY ( 6 FDA reports)
SOMATOFORM DISORDER ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
TOOTH LOSS ( 6 FDA reports)
TOXIC DILATATION OF COLON ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
VAGINAL HAEMORRHAGE ( 6 FDA reports)
VEIN DISORDER ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
WATER INTOXICATION ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
AFFECT LABILITY ( 5 FDA reports)
ALCOHOL USE ( 5 FDA reports)
AMENORRHOEA ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
APHASIA ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 5 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHRONIC SINUSITIS ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DEMENTIA ( 5 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DILATATION VENTRICULAR ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
DYSPHORIA ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FEELING OF DESPAIR ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
GENERALISED ERYTHEMA ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMOGLOBIN INCREASED ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOPROTEINAEMIA ( 5 FDA reports)
LIMB MALFORMATION ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
MOOD ALTERED ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MYOCARDIAL FIBROSIS ( 5 FDA reports)
PETECHIAE ( 5 FDA reports)
PREMATURE LABOUR ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SENSATION OF HEAVINESS ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
STRESS ( 5 FDA reports)
SURGERY ( 5 FDA reports)
SWELLING ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
ABORTION INCOMPLETE ( 4 FDA reports)
ACIDOSIS ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANURIA ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BREAST MASS ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CARDIOVERSION ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DECREASED INTEREST ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DEVELOPMENTAL DELAY ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
GARDNERELLA INFECTION ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
LARYNGEAL DISORDER ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENSTRUATION IRREGULAR ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
NEGATIVISM ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
PANIC DISORDER ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RALES ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
RESTLESS LEGS SYNDROME ( 4 FDA reports)
SCAB ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
STRABISMUS ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
TOBACCO USER ( 4 FDA reports)
TONGUE SPASM ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ABORTION ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ALCOHOLIC LIVER DISEASE ( 3 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 3 FDA reports)
AMIMIA ( 3 FDA reports)
ANTISOCIAL BEHAVIOUR ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BOWEL SOUNDS ABNORMAL ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC DISCOMFORT ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLITIS ULCERATIVE ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
COMA ACIDOTIC ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
ESCHERICHIA VAGINITIS ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FOETAL HEART RATE ABNORMAL ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HALLUCINATION, OLFACTORY ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INDURATION ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
JOINT HYPEREXTENSION ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MASS ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEAN CELL VOLUME INCREASED ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOFASCITIS ( 3 FDA reports)
NEONATAL ASPHYXIA ( 3 FDA reports)
NORMAL NEWBORN ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OCULOGYRATION ( 3 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PARKINSONIAN CRISIS ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PARTNER STRESS ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PHLEBOTHROMBOSIS ( 3 FDA reports)
PHOBIA ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
POTENTIATING DRUG INTERACTION ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PSYCHOMOTOR AGITATION ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TINEA PEDIS ( 3 FDA reports)
TONIC CONVULSION ( 3 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
VAGINITIS GARDNERELLA ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
XANTHOMA ( 3 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABNORMAL CHEST SOUND ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASPIRATION TRACHEAL ( 2 FDA reports)
ATRIOVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD ANTIDIURETIC HORMONE ABNORMAL ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DISUSE SYNDROME ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
EJACULATION DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCONVULSIVE THERAPY ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOETAL MACROSOMIA ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FUMBLING ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLUCOSE URINE ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERPHOSPHATASAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPERVIGILANCE ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
HYSTERICAL PSYCHOSIS ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
MACROPHAGE ACTIVATION ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MACULAR OEDEMA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORCHITIS NONINFECTIVE ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
PSYCHOLOGICAL FACTOR AFFECTING MEDICAL CONDITION ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY HAEMOSIDEROSIS ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SOMNOLENCE NEONATAL ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STIFF PERSON SYNDROME ( 2 FDA reports)
STRAWBERRY TONGUE ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
URINE POTASSIUM DECREASED ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
APGAR SCORE ABNORMAL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMATOMA ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BASAL GANGLION DEGENERATION ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLAST CELL COUNT DECREASED ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRACHIAL PLEXOPATHY ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL LOBOTOMY ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CSF OLIGOCLONAL BAND PRESENT ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DROP ATTACKS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLOPPY EYELID SYNDROME ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRIC ADENOMA ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GLASGOW COMA SCALE ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIVE ANEURYSM ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEGACOLON ACQUIRED ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL DEPRESSION ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING OESOPHAGITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL ACHALASIA ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL DRAINAGE TEST ABNORMAL ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYNEUROPATHY ALCOHOLIC ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATIC ABSCESS ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HILUM MASS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
SALT INTOXICATION ( 1 FDA reports)
SCHIZOPHRENIA, CATATONIC TYPE ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SEROLOGY NEGATIVE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DEGENERATIVE DISORDER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL ANAESTHESIA ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYDENHAM'S CHOREA ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THREATENED LABOUR ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
TIC ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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