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

PYREXIA ( 37 FDA reports)
OVERDOSE ( 35 FDA reports)
COMPLETED SUICIDE ( 29 FDA reports)
DEPRESSION ( 28 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 25 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 25 FDA reports)
CONVULSION ( 24 FDA reports)
MALAISE ( 24 FDA reports)
ANAEMIA ( 23 FDA reports)
RHABDOMYOLYSIS ( 23 FDA reports)
SOMNOLENCE ( 23 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 22 FDA reports)
INSOMNIA ( 22 FDA reports)
RENAL FAILURE ACUTE ( 22 FDA reports)
ANXIETY ( 21 FDA reports)
DRUG INEFFECTIVE ( 20 FDA reports)
DRUG INTERACTION ( 20 FDA reports)
IRRITABILITY ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 19 FDA reports)
SEROTONIN SYNDROME ( 19 FDA reports)
ARTHRALGIA ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
PAIN ( 18 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
LOSS OF CONSCIOUSNESS ( 17 FDA reports)
SUICIDAL IDEATION ( 17 FDA reports)
SUICIDE ATTEMPT ( 17 FDA reports)
TACHYCARDIA ( 16 FDA reports)
DYSPNOEA ( 15 FDA reports)
HEART RATE INCREASED ( 15 FDA reports)
INTENTIONAL OVERDOSE ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
STATUS EPILEPTICUS ( 15 FDA reports)
BLOOD PRESSURE DECREASED ( 14 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
DIARRHOEA ( 14 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
DIZZINESS ( 13 FDA reports)
LIVER DISORDER ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
PLATELET COUNT DECREASED ( 13 FDA reports)
PULMONARY OEDEMA ( 13 FDA reports)
RASH ( 13 FDA reports)
TREMOR ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 12 FDA reports)
CONFUSIONAL STATE ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
URINARY TRACT INFECTION ( 12 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 11 FDA reports)
CLONIC CONVULSION ( 11 FDA reports)
DELIRIUM ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 11 FDA reports)
TACHYPNOEA ( 11 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 11 FDA reports)
ANOREXIA ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
CONSTIPATION ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
GENERALISED OEDEMA ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ( 10 FDA reports)
MUSCLE RIGIDITY ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
VOMITING ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 10 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
FALL ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HEART RATE DECREASED ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
HYPERPYREXIA ( 9 FDA reports)
INFECTION ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
SHOCK ( 9 FDA reports)
BACK PAIN ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 8 FDA reports)
DEATH ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DIABETIC KETOACIDOSIS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
RESTLESSNESS ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ACIDOSIS ( 7 FDA reports)
ACTIVATION SYNDROME ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
ATELECTASIS ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
CELLULITIS ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
PULMONARY CONGESTION ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 6 FDA reports)
AORTIC DILATATION ( 6 FDA reports)
APATHY ( 6 FDA reports)
ASTHENOSPERMIA ( 6 FDA reports)
AZOOSPERMIA ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD OSMOLARITY DECREASED ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
EARLY MORNING AWAKENING ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
GALACTORRHOEA ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
HAEMOLYTIC ANAEMIA ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERPLASIA ( 6 FDA reports)
HYPOAESTHESIA ORAL ( 6 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 6 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 6 FDA reports)
JOINT EFFUSION ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MULTIPLE MYELOMA ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
ORAL CAVITY FISTULA ( 6 FDA reports)
ORAL DISORDER ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PARKINSONISM ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SEPSIS SYNDROME ( 6 FDA reports)
SPERMATOGENESIS ABNORMAL ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TOOTH ABSCESS ( 6 FDA reports)
ABULIA ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ASPHYXIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CEREBROVASCULAR DISORDER ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
MYOCLONUS ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BREAST ENLARGEMENT ( 4 FDA reports)
CHILLS ( 4 FDA reports)
COMA SCALE ABNORMAL ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RETINOPATHY ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
AKATHISIA ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APHONIA ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BRAIN NEOPLASM ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHOKING ( 3 FDA reports)
COUGH ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MANIA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MONOCYTE COUNT INCREASED ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
POISONING ( 3 FDA reports)
PORIOMANIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
SCREAMING ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TEARFULNESS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANGER ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
EJACULATION FAILURE ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPULSE-CONTROL DISORDER ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PATELLA REPLACEMENT ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL ABSCESS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUMOUR MARKER INCREASED ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URTICARIA CHRONIC ( 2 FDA reports)
VAGINITIS GARDNERELLA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
AURA ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD CAFFEINE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
POLYP ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RHINITIS SEASONAL ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREMOR NEONATAL ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URACHAL ABSCESS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTOUSE EXTRACTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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