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

MALAISE ( 25 FDA reports)
OVERDOSE ( 25 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 25 FDA reports)
PSYCHOTIC DISORDER ( 24 FDA reports)
COMA ( 23 FDA reports)
COMPLETED SUICIDE ( 22 FDA reports)
DRUG INTERACTION ( 21 FDA reports)
DEATH ( 20 FDA reports)
SOMNOLENCE ( 20 FDA reports)
AGITATION ( 19 FDA reports)
NAUSEA ( 19 FDA reports)
NEUTROPENIA ( 19 FDA reports)
RHABDOMYOLYSIS ( 19 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 18 FDA reports)
DRUG TOXICITY ( 18 FDA reports)
MULTIPLE DRUG OVERDOSE ( 18 FDA reports)
CONFUSIONAL STATE ( 16 FDA reports)
HALLUCINATION ( 16 FDA reports)
HALLUCINATION, AUDITORY ( 16 FDA reports)
SUICIDE ATTEMPT ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 16 FDA reports)
AGGRESSION ( 15 FDA reports)
SUICIDAL IDEATION ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
DIARRHOEA ( 14 FDA reports)
NEUTROPHIL COUNT INCREASED ( 14 FDA reports)
VOMITING ( 14 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
ANXIETY ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
PNEUMONIA ( 12 FDA reports)
QUALITY OF LIFE DECREASED ( 12 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
DIZZINESS ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
SEDATION ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DIABETES MELLITUS ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 8 FDA reports)
OXYGEN SATURATION DECREASED ( 8 FDA reports)
POISONING ( 8 FDA reports)
UNRESPONSIVE TO STIMULI ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
INTENTIONAL OVERDOSE ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
MENTAL IMPAIRMENT ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
SCHIZOPHRENIA ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
ASTROCYTOMA ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
BRAIN OPERATION ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
FALL ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
MANIA ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANGER ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DRUG DEPENDENCE ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOMANIA ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
METASTASIS ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PHYSICAL ASSAULT ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POLYSUBSTANCE ABUSE ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RASH ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
STRESS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
APATHY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONGENITAL RENAL DISORDER ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENITAL INJURY ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OESTRADIOL DECREASED ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARANASAL CYST ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SOMATIC HALLUCINATION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLIC PSYCHOSIS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PH ABNORMAL ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF ESTEEM INFLATED ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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