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

DRUG INTERACTION ( 37 FDA reports)
PLATELET COUNT DECREASED ( 28 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 25 FDA reports)
BREAST ABSCESS ( 22 FDA reports)
METASTASES TO SPINE ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
NEUTROPENIA ( 15 FDA reports)
BREAST CANCER ( 13 FDA reports)
MENTAL IMPAIRMENT ( 13 FDA reports)
ABSCESS ( 12 FDA reports)
NEUTROPHIL COUNT INCREASED ( 12 FDA reports)
BLOOD PROLACTIN INCREASED ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 10 FDA reports)
HALLUCINATION, AUDITORY ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BREAST CANCER FEMALE ( 6 FDA reports)
BREAST CANCER METASTATIC ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RASH ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 4 FDA reports)
OVARIAN ADENOMA ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MALAISE ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
SUBACUTE ENDOCARDITIS ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
AGITATION ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
APATHY ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FALL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POSTURING ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTRALATERAL BREAST CANCER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OVARIAN FIBROMA ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PELVIC ADHESIONS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THOUGHT BROADCASTING ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TIC ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WAXY FLEXIBILITY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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