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

PYREXIA ( 52 FDA reports)
IRRITABILITY ( 27 FDA reports)
LOSS OF CONSCIOUSNESS ( 26 FDA reports)
RHABDOMYOLYSIS ( 23 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 21 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 21 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 20 FDA reports)
SEROTONIN SYNDROME ( 19 FDA reports)
VOMITING ( 18 FDA reports)
BLOOD PRESSURE DECREASED ( 17 FDA reports)
DRUG ERUPTION ( 16 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
SOMNOLENCE ( 15 FDA reports)
DIZZINESS ( 14 FDA reports)
CONVULSION ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
PLATELET COUNT DECREASED ( 13 FDA reports)
SUICIDE ATTEMPT ( 13 FDA reports)
FEELING ABNORMAL ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
RASH ( 12 FDA reports)
AGGRESSION ( 11 FDA reports)
ABDOMINAL PAIN UPPER ( 10 FDA reports)
ANAEMIA ( 10 FDA reports)
ANXIETY ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
HAEMATOCHEZIA ( 10 FDA reports)
MALAISE ( 10 FDA reports)
TACHYCARDIA ( 10 FDA reports)
TREMOR ( 10 FDA reports)
INTENTIONAL OVERDOSE ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
MYOCLONUS ( 9 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
FALL ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
PARKINSONISM ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SMALL INTESTINAL PERFORATION ( 8 FDA reports)
TONIC CONVULSION ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
ARTERIAL STENT INSERTION ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
ENTEROSTOMY ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
OESOPHAGOSTOMY ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
STENT REMOVAL ( 7 FDA reports)
SURGERY ( 7 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CHILLS ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
FEELING DRUNK ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GENERALISED OEDEMA ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
OESOPHAGEAL PERFORATION ( 6 FDA reports)
OVARIAN CANCER ( 6 FDA reports)
PAIN ( 6 FDA reports)
STUPOR ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 5 FDA reports)
DYSLALIA ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
GLOSSOPTOSIS ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NECROSIS ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ASTHENOSPERMIA ( 4 FDA reports)
AZOOSPERMIA ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
EYELID FUNCTION DISORDER ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEEDING DISORDER NEONATAL ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
MANIA ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 4 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 4 FDA reports)
XERODERMA ( 4 FDA reports)
ABDOMINAL OBESITY ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
APATHY ( 3 FDA reports)
APNOEA ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOVENTILATION NEONATAL ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
PHOBIA ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
ANGER ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
COMA ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
INADEQUATE ANALGESIA ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RETINAL DEPIGMENTATION ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SOMNOLENCE NEONATAL ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
TENSION ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEAR OF ANIMALS ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPID METABOLISM DISORDER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POISONING ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THEFT ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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