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

WHITE BLOOD CELL COUNT INCREASED ( 189 FDA reports)
DRUG INTERACTION ( 158 FDA reports)
PLATELET COUNT DECREASED ( 145 FDA reports)
MENTAL IMPAIRMENT ( 134 FDA reports)
NEUTROPHIL COUNT INCREASED ( 122 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 116 FDA reports)
NEUTROPENIA ( 112 FDA reports)
PSYCHOTIC DISORDER ( 112 FDA reports)
VOMITING ( 110 FDA reports)
BREAST ABSCESS ( 106 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 105 FDA reports)
BREAST CANCER ( 102 FDA reports)
HAEMOGLOBIN DECREASED ( 102 FDA reports)
PNEUMONIA ( 100 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 99 FDA reports)
METASTASES TO SPINE ( 98 FDA reports)
NEUTROPHIL COUNT DECREASED ( 98 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 96 FDA reports)
MALAISE ( 96 FDA reports)
TACHYCARDIA ( 87 FDA reports)
CONFUSIONAL STATE ( 84 FDA reports)
BLOOD PROLACTIN INCREASED ( 82 FDA reports)
SOMNOLENCE ( 82 FDA reports)
AGITATION ( 74 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 73 FDA reports)
OVERDOSE ( 72 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 69 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 68 FDA reports)
SALIVARY HYPERSECRETION ( 68 FDA reports)
ABSCESS ( 67 FDA reports)
DRUG INEFFECTIVE ( 66 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 65 FDA reports)
DYSPNOEA ( 64 FDA reports)
HYPERTENSION ( 64 FDA reports)
HALLUCINATION, AUDITORY ( 61 FDA reports)
PYREXIA ( 61 FDA reports)
SPEECH DISORDER ( 60 FDA reports)
ABNORMAL BEHAVIOUR ( 59 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 59 FDA reports)
HYPERHIDROSIS ( 59 FDA reports)
DIARRHOEA ( 56 FDA reports)
PARANOIA ( 55 FDA reports)
LOSS OF CONSCIOUSNESS ( 53 FDA reports)
BLOOD BILIRUBIN INCREASED ( 52 FDA reports)
WEIGHT DECREASED ( 52 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 51 FDA reports)
HYPOTHYROIDISM ( 51 FDA reports)
BODY TEMPERATURE INCREASED ( 48 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 48 FDA reports)
RHABDOMYOLYSIS ( 47 FDA reports)
DIZZINESS ( 46 FDA reports)
LEUKOPENIA ( 46 FDA reports)
OVARIAN ADENOMA ( 46 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 45 FDA reports)
SCHIZOPHRENIA ( 45 FDA reports)
DEPRESSION ( 44 FDA reports)
HEART RATE INCREASED ( 44 FDA reports)
AGGRESSION ( 43 FDA reports)
FATIGUE ( 43 FDA reports)
WEIGHT INCREASED ( 43 FDA reports)
CHEST PAIN ( 42 FDA reports)
DEATH ( 41 FDA reports)
ASTHENIA ( 40 FDA reports)
CONDITION AGGRAVATED ( 40 FDA reports)
CONSTIPATION ( 39 FDA reports)
RENAL IMPAIRMENT ( 39 FDA reports)
SEDATION ( 39 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 38 FDA reports)
CARDIAC ARREST ( 38 FDA reports)
DRUG TOXICITY ( 37 FDA reports)
FALL ( 37 FDA reports)
MENTAL DISORDER ( 37 FDA reports)
CONVULSION ( 36 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 35 FDA reports)
SEPSIS ( 34 FDA reports)
RASH ( 33 FDA reports)
ANXIETY ( 32 FDA reports)
NAUSEA ( 32 FDA reports)
RENAL FAILURE ( 32 FDA reports)
AGRANULOCYTOSIS ( 31 FDA reports)
DELUSION ( 31 FDA reports)
HYPOTENSION ( 31 FDA reports)
PULMONARY EMBOLISM ( 31 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 29 FDA reports)
CIRCULATORY COLLAPSE ( 29 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 29 FDA reports)
BLOOD PRESSURE INCREASED ( 28 FDA reports)
DISTURBANCE IN ATTENTION ( 28 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 27 FDA reports)
INTENTIONAL OVERDOSE ( 27 FDA reports)
RENAL FAILURE ACUTE ( 27 FDA reports)
DEPRESSED MOOD ( 26 FDA reports)
HEPATIC STEATOSIS ( 26 FDA reports)
INSOMNIA ( 26 FDA reports)
RESPIRATORY FAILURE ( 26 FDA reports)
THROMBOCYTOPENIA ( 26 FDA reports)
URINARY INCONTINENCE ( 26 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 25 FDA reports)
DEEP VEIN THROMBOSIS ( 25 FDA reports)
DRUG LEVEL INCREASED ( 25 FDA reports)
TREMOR ( 25 FDA reports)
IMPAIRED SELF-CARE ( 24 FDA reports)
DEHYDRATION ( 23 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 23 FDA reports)
GASTRITIS ( 23 FDA reports)
NOCTURIA ( 23 FDA reports)
URINARY TRACT INFECTION ( 23 FDA reports)
WAXY FLEXIBILITY ( 23 FDA reports)
HEADACHE ( 22 FDA reports)
SUDDEN DEATH ( 22 FDA reports)
ABDOMINAL PAIN ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
GRAND MAL CONVULSION ( 21 FDA reports)
INFLUENZA LIKE ILLNESS ( 21 FDA reports)
OROPHARYNGEAL PAIN ( 21 FDA reports)
SINUS TACHYCARDIA ( 21 FDA reports)
SLEEP DISORDER ( 21 FDA reports)
TREATMENT NONCOMPLIANCE ( 21 FDA reports)
DIABETES MELLITUS ( 20 FDA reports)
HYPOMANIA ( 20 FDA reports)
PANCREATITIS ( 20 FDA reports)
POSTURE ABNORMAL ( 20 FDA reports)
POSTURING ( 20 FDA reports)
ANTISOCIAL BEHAVIOUR ( 19 FDA reports)
DISORIENTATION ( 19 FDA reports)
GAIT DISTURBANCE ( 19 FDA reports)
HALLUCINATION, VISUAL ( 19 FDA reports)
MYOCARDIAL INFARCTION ( 19 FDA reports)
POLLAKIURIA ( 19 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 18 FDA reports)
CHOLINERGIC SYNDROME ( 18 FDA reports)
DYSPHAGIA ( 18 FDA reports)
FEELING ABNORMAL ( 18 FDA reports)
ILLUSION ( 18 FDA reports)
MOOD ALTERED ( 18 FDA reports)
MUSCLE RIGIDITY ( 18 FDA reports)
PHYSICAL ASSAULT ( 18 FDA reports)
SLEEP APNOEA SYNDROME ( 18 FDA reports)
EOSINOPHIL COUNT INCREASED ( 17 FDA reports)
HALLUCINATION ( 17 FDA reports)
NEOPLASM MALIGNANT ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
ARTHRITIS ( 16 FDA reports)
DISINHIBITION ( 16 FDA reports)
HYPERPROLACTINAEMIA ( 16 FDA reports)
OXYGEN SATURATION DECREASED ( 16 FDA reports)
PLATELET COUNT INCREASED ( 16 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 15 FDA reports)
BALANCE DISORDER ( 15 FDA reports)
CARDIOMYOPATHY ( 15 FDA reports)
DECREASED APPETITE ( 15 FDA reports)
INFECTION ( 15 FDA reports)
MONOCYTE COUNT INCREASED ( 15 FDA reports)
MYOCLONUS ( 15 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 15 FDA reports)
SPLENOMEGALY ( 15 FDA reports)
SUICIDE ATTEMPT ( 15 FDA reports)
TARDIVE DYSKINESIA ( 15 FDA reports)
ATRIAL FIBRILLATION ( 14 FDA reports)
COUGH ( 14 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 14 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 14 FDA reports)
DYSTONIA ( 14 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 14 FDA reports)
H1N1 INFLUENZA ( 14 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
LEUKOCYTOSIS ( 14 FDA reports)
MOBILITY DECREASED ( 14 FDA reports)
NASOPHARYNGITIS ( 14 FDA reports)
PAIN ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 14 FDA reports)
SUICIDAL IDEATION ( 14 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
HAEMORRHOIDS ( 13 FDA reports)
HYPERTHYROIDISM ( 13 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 13 FDA reports)
MANIA ( 13 FDA reports)
MUTISM ( 13 FDA reports)
OVERWEIGHT ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
BLOOD UREA INCREASED ( 12 FDA reports)
CARDIAC DISORDER ( 12 FDA reports)
DYSARTHRIA ( 12 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
ORTHOSTATIC HYPOTENSION ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
SCHIZOPHRENIA, CATATONIC TYPE ( 12 FDA reports)
STARING ( 12 FDA reports)
URINARY RETENTION ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 11 FDA reports)
CATATONIA ( 11 FDA reports)
COGNITIVE DISORDER ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
FAECAL INCONTINENCE ( 11 FDA reports)
HAEMATOCRIT INCREASED ( 11 FDA reports)
IMPULSIVE BEHAVIOUR ( 11 FDA reports)
JOINT DISLOCATION ( 11 FDA reports)
LETHARGY ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
LUNG NEOPLASM MALIGNANT ( 11 FDA reports)
MYOSITIS ( 11 FDA reports)
ORCHITIS ( 11 FDA reports)
POLYCYTHAEMIA ( 11 FDA reports)
PULMONARY CONGESTION ( 11 FDA reports)
RASH GENERALISED ( 11 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 11 FDA reports)
SENSORY DISTURBANCE ( 11 FDA reports)
TEARFULNESS ( 11 FDA reports)
THINKING ABNORMAL ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 11 FDA reports)
VEIN DISORDER ( 11 FDA reports)
VITAMIN D DECREASED ( 11 FDA reports)
ABDOMINAL DISCOMFORT ( 10 FDA reports)
AMENORRHOEA ( 10 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
ASPIRATION ( 10 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
BRONCHITIS ( 10 FDA reports)
CARDIOGENIC SHOCK ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
DECREASED INTEREST ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
ENCEPHALOPATHY ( 10 FDA reports)
FAECALOMA ( 10 FDA reports)
HAEMATOCRIT DECREASED ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 10 FDA reports)
METABOLIC DISORDER ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ( 10 FDA reports)
OBESITY ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
SUBACUTE ENDOCARDITIS ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CELLULITIS ( 9 FDA reports)
DYSKINESIA ( 9 FDA reports)
DYSPHORIA ( 9 FDA reports)
EAR INFECTION ( 9 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
MYOCARDIAL ISCHAEMIA ( 9 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
RESPIRATORY DEPRESSION ( 9 FDA reports)
RESTLESS LEGS SYNDROME ( 9 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 9 FDA reports)
SPUTUM DISCOLOURED ( 9 FDA reports)
AMMONIA INCREASED ( 8 FDA reports)
ARTHRALGIA ( 8 FDA reports)
BLOOD CALCIUM DECREASED ( 8 FDA reports)
BLOOD UREA DECREASED ( 8 FDA reports)
COLITIS ( 8 FDA reports)
COMA ( 8 FDA reports)
COMA SCALE ABNORMAL ( 8 FDA reports)
DRUG ABUSE ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
EPILEPSY ( 8 FDA reports)
HAEMOGLOBIN INCREASED ( 8 FDA reports)
HYPERTENSIVE HEART DISEASE ( 8 FDA reports)
MOVEMENT DISORDER ( 8 FDA reports)
RASH MACULO-PAPULAR ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
WOUND INFECTION ( 8 FDA reports)
ACUTE PSYCHOSIS ( 7 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
CHILLS ( 7 FDA reports)
CHOKING ( 7 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HEPATIC ENZYME INCREASED ( 7 FDA reports)
HYDRONEPHROSIS ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
HYPOKINESIA ( 7 FDA reports)
IMMOBILE ( 7 FDA reports)
INTESTINAL INFARCTION ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
MICROCYTIC ANAEMIA ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NEPHRITIS INTERSTITIAL ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PITUITARY TUMOUR BENIGN ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PSYCHOMOTOR RETARDATION ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
STRESS ( 7 FDA reports)
TRACHEOSTOMY ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ADVERSE DRUG REACTION ( 6 FDA reports)
APATHY ( 6 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 6 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CONJUNCTIVAL DISORDER ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DIABETIC KETOACIDOSIS ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HALLUCINATIONS, MIXED ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
HYPOTONIA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
INJURY ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NEPHRITIS ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
POOR PERSONAL HYGIENE ( 6 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SHOCK ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
WITHDRAWAL SYNDROME ( 6 FDA reports)
AFFECTIVE DISORDER ( 5 FDA reports)
ANGER ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
BLOOD COUNT ABNORMAL ( 5 FDA reports)
BLOOD DISORDER ( 5 FDA reports)
BREAST CANCER FEMALE ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CARDIAC HYPERTROPHY ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
COMMUNICATION DISORDER ( 5 FDA reports)
CONTUSION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 5 FDA reports)
EOSINOPHIL COUNT DECREASED ( 5 FDA reports)
EPIDIDYMAL INFECTION ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
FACIAL BONES FRACTURE ( 5 FDA reports)
FEAR ( 5 FDA reports)
GALACTORRHOEA ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPOPHAGIA ( 5 FDA reports)
IMPAIRED WORK ABILITY ( 5 FDA reports)
INCONTINENCE ( 5 FDA reports)
INTESTINAL ISCHAEMIA ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
MYOCARDITIS ( 5 FDA reports)
MYOGLOBINURIA ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
POOR VENOUS ACCESS ( 5 FDA reports)
POVERTY OF SPEECH ( 5 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 5 FDA reports)
SOPOR ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
TIC ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APPARENT DEATH ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BRADYPHRENIA ( 4 FDA reports)
BREAST CANCER METASTATIC ( 4 FDA reports)
BRUXISM ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
COMPULSIONS ( 4 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DECREASED EYE CONTACT ( 4 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
EJECTION FRACTION ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA ( 4 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HYPERKINETIC HEART SYNDROME ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOGONADISM ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LIBIDO DECREASED ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MONOCYTE COUNT ABNORMAL ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NECROTISING COLITIS ( 4 FDA reports)
NEGATIVISM ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OTORRHOEA ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PARKINSON'S DISEASE ( 4 FDA reports)
PERSECUTORY DELUSION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PSYCHOTIC BEHAVIOUR ( 4 FDA reports)
PULSE ABNORMAL ( 4 FDA reports)
RALES ( 4 FDA reports)
RENAL HYPERTENSION ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 4 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 4 FDA reports)
SUBSTANCE ABUSE ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SUSPICIOUSNESS ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 4 FDA reports)
TERMINAL STATE ( 4 FDA reports)
TONGUE BITING ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TROPONIN I INCREASED ( 4 FDA reports)
URINARY TRACT OBSTRUCTION ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
ALCOHOL ABUSE ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CATAPLEXY ( 3 FDA reports)
CATECHOLAMINES URINE INCREASED ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DELUSIONAL PERCEPTION ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DROP ATTACKS ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELEVATED MOOD ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
EPIDIDYMAL DISORDER ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAND DEFORMITY ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEUTROPHILIA ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PATHOLOGICAL GAMBLING ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 3 FDA reports)
SCAR ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN INFECTION ( 3 FDA reports)
SOCIAL PROBLEM ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TEMPORAL LOBE EPILEPSY ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER OBSTRUCTION ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TEST ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHOSCOPY ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLONIC ATONY ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CRYING ( 2 FDA reports)
CRYPTORCHISM ( 2 FDA reports)
CSF GLUCOSE ABNORMAL ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FAECAL DISIMPACTION ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HEAD BANGING ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
ILEECTOMY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
JOINT CREPITATION ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LARGE FOR DATES BABY ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIP ULCERATION ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MASKED FACIES ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS SALMONELLA ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO KIDNEY ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
NEGATIVE THOUGHTS ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
PROTEIN C DECREASED ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RESECTION OF RECTUM ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SKIN ULCER EXCISION ( 2 FDA reports)
SOMATIC HALLUCINATION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STIFF-MAN SYNDROME ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
THERAPY CESSATION ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
TOBACCO USER ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA 1 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIOPSY BONE MARROW ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL CYSTIC LUNG ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DUODENAL SPHINCTEROTOMY ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSMORPHOPHOBIA ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLIGHT OF IDEAS ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEAD TITUBATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MENINGITIS MENINGOCOCCAL ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC ORGAN INJURY ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PINEAL GERMINOMA ( 1 FDA reports)
PINEALOBLASTOMA ( 1 FDA reports)
PINEOCYTOMA ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
RABBIT SYNDROME ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
URETHROTOMY ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VANILLYL MANDELIC ACID URINE INCREASED ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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