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

DRUG EXPOSURE DURING PREGNANCY ( 147 FDA reports)
NAUSEA ( 77 FDA reports)
DRUG INTERACTION ( 76 FDA reports)
ABORTION SPONTANEOUS ( 69 FDA reports)
BLOOD BILIRUBIN INCREASED ( 69 FDA reports)
DIARRHOEA ( 68 FDA reports)
PREMATURE BABY ( 54 FDA reports)
RENAL FAILURE ACUTE ( 53 FDA reports)
HEADACHE ( 49 FDA reports)
PYREXIA ( 48 FDA reports)
HYPERBILIRUBINAEMIA ( 45 FDA reports)
VOMITING ( 44 FDA reports)
ANAEMIA ( 38 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 36 FDA reports)
PREGNANCY ( 36 FDA reports)
LIPODYSTROPHY ACQUIRED ( 35 FDA reports)
DYSPNOEA ( 32 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 32 FDA reports)
ABDOMINAL PAIN ( 30 FDA reports)
KAPOSI'S SARCOMA ( 28 FDA reports)
RASH ( 28 FDA reports)
HEPATIC CIRRHOSIS ( 27 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 26 FDA reports)
NEPHROLITHIASIS ( 26 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 26 FDA reports)
HEPATITIS ACUTE ( 25 FDA reports)
LIPOATROPHY ( 25 FDA reports)
NEPHRITIS INTERSTITIAL ( 25 FDA reports)
RENAL FAILURE ( 25 FDA reports)
NEUROPATHY PERIPHERAL ( 24 FDA reports)
ABORTION INDUCED ( 23 FDA reports)
DEPRESSION ( 23 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
HYPERGLYCAEMIA ( 22 FDA reports)
PLATELET COUNT DECREASED ( 22 FDA reports)
RENAL IMPAIRMENT ( 22 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 22 FDA reports)
FATIGUE ( 21 FDA reports)
HAEMOGLOBIN DECREASED ( 21 FDA reports)
HEPATITIS C ( 21 FDA reports)
TRISOMY 21 ( 21 FDA reports)
ATRIAL SEPTAL DEFECT ( 20 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 20 FDA reports)
HYPERLIPIDAEMIA ( 20 FDA reports)
CHOLELITHIASIS ( 19 FDA reports)
DEATH ( 19 FDA reports)
PNEUMONIA ( 19 FDA reports)
SEPSIS ( 19 FDA reports)
VISION BLURRED ( 19 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
DIABETES MELLITUS ( 18 FDA reports)
HYDROCEPHALUS ( 18 FDA reports)
HYPOAESTHESIA FACIAL ( 18 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 18 FDA reports)
JAUNDICE ( 17 FDA reports)
MALAISE ( 17 FDA reports)
MITRAL VALVE INCOMPETENCE ( 17 FDA reports)
PARKINSONISM ( 17 FDA reports)
STILLBIRTH ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 17 FDA reports)
ASCITES ( 16 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
HAEMATOCHEZIA ( 16 FDA reports)
HEPATITIS ( 16 FDA reports)
RHABDOMYOLYSIS ( 16 FDA reports)
TORSADE DE POINTES ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 15 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 15 FDA reports)
INFLUENZA LIKE ILLNESS ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
STAPHYLOCOCCAL INFECTION ( 15 FDA reports)
VENTRICULAR TACHYCARDIA ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
FALLOT'S TETRALOGY ( 14 FDA reports)
HAEMOLYTIC ANAEMIA ( 14 FDA reports)
HEPATIC ENZYME INCREASED ( 14 FDA reports)
HYPERTHERMIA ( 14 FDA reports)
LYMPHOMA ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
PAIN ( 14 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 14 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 14 FDA reports)
RENAL TUBULAR NECROSIS ( 14 FDA reports)
ARTHRALGIA ( 13 FDA reports)
CONVULSION ( 13 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 13 FDA reports)
DRUG RESISTANCE ( 13 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
MELAENA ( 13 FDA reports)
NEPHROTIC SYNDROME ( 13 FDA reports)
PRE-ECLAMPSIA ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 12 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 12 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
CARDIAC MURMUR ( 12 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 12 FDA reports)
DIZZINESS ( 12 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
HEPATIC STEATOSIS ( 12 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 12 FDA reports)
MICROCEPHALY ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 12 FDA reports)
VARICES OESOPHAGEAL ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 11 FDA reports)
BRADYCARDIA ( 11 FDA reports)
COMA ( 11 FDA reports)
CUSHING'S SYNDROME ( 11 FDA reports)
DECREASED APPETITE ( 11 FDA reports)
ENCEPHALITIS ( 11 FDA reports)
HEPATOMEGALY ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
SPLENOMEGALY ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
TRANSAMINASES INCREASED ( 11 FDA reports)
ACROCHORDON ( 10 FDA reports)
CACHEXIA ( 10 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 10 FDA reports)
COUGH ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HAEMATURIA ( 10 FDA reports)
HEPATOSPLENOMEGALY ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
PREMATURE LABOUR ( 10 FDA reports)
PROTEINURIA ( 10 FDA reports)
PULMONARY INFARCTION ( 10 FDA reports)
TREMOR ( 10 FDA reports)
VIRAL LOAD INCREASED ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
CARDIO-RESPIRATORY ARREST ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DEVELOPMENTAL DELAY ( 9 FDA reports)
EYELID PTOSIS ( 9 FDA reports)
GUILLAIN-BARRE SYNDROME ( 9 FDA reports)
HEART DISEASE CONGENITAL ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
PANCREATITIS ACUTE ( 9 FDA reports)
PLACENTAL DISORDER ( 9 FDA reports)
PORTAL VEIN THROMBOSIS ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ANGINA UNSTABLE ( 8 FDA reports)
AORTIC VALVE INCOMPETENCE ( 8 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
ECLAMPSIA ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
HEART SOUNDS ABNORMAL ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
LIVE BIRTH ( 8 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
METABOLIC ACIDOSIS ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
NORMAL NEWBORN ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
PULMONARY TUBERCULOSIS ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
RENAL TUBULAR DISORDER ( 8 FDA reports)
SMALL FOR DATES BABY ( 8 FDA reports)
SOMNAMBULISM ( 8 FDA reports)
TREATMENT NONCOMPLIANCE ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
AGITATION ( 7 FDA reports)
AIDS ENCEPHALOPATHY ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
DRUG ABUSE ( 7 FDA reports)
DRUG LEVEL INCREASED ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
FANCONI SYNDROME ACQUIRED ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
GLAUCOMA ( 7 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 7 FDA reports)
HYPERURICAEMIA ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
INTESTINAL PERFORATION ( 7 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
MASS ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 7 FDA reports)
PERITONITIS ( 7 FDA reports)
PLACENTAL INSUFFICIENCY ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
RETINOPATHY OF PREMATURITY ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
VIITH NERVE PARALYSIS ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ALCOHOL INTERACTION ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 6 FDA reports)
ARTHRITIS BACTERIAL ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
CASTLEMAN'S DISEASE ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 6 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
EROSIVE DUODENITIS ( 6 FDA reports)
FOETAL DISTRESS SYNDROME ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
GASTROENTERITIS VIRAL ( 6 FDA reports)
GLYCOSURIA ( 6 FDA reports)
HEPATIC LESION ( 6 FDA reports)
HIV INFECTION ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
NIGHTMARE ( 6 FDA reports)
PLACENTA PRAEVIA ( 6 FDA reports)
PYELECTASIA ( 6 FDA reports)
RENAL DYSPLASIA ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
TALIPES ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
UVEITIS ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
VIROLOGIC FAILURE ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
APHASIA ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
BLOOD HIV RNA INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CAESAREAN SECTION ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CHORIOAMNIONITIS ( 5 FDA reports)
CLEFT LIP ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CONGENITAL HYDROCEPHALUS ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 5 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
FALL ( 5 FDA reports)
FAT TISSUE INCREASED ( 5 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 5 FDA reports)
FOETAL GROWTH RETARDATION ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HERPES ZOSTER ( 5 FDA reports)
HYPERLACTACIDAEMIA ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPERVENTILATION ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
HYPOPHOSPHATAEMIA ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
MENINGISM ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
MOANING ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
NEURODEGENERATIVE DISORDER ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 5 FDA reports)
OFF LABEL USE ( 5 FDA reports)
PLEURAL ADHESION ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PNEUMONIA BACTERIAL ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PULMONARY HYPERTENSION ( 5 FDA reports)
RENAL COLIC ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
BACTERAEMIA ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CONDUCTION DISORDER ( 4 FDA reports)
CONGENITAL NAEVUS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 4 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FANCONI SYNDROME ( 4 FDA reports)
FEBRILE BONE MARROW APLASIA ( 4 FDA reports)
FINE MOTOR DELAY ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERKERATOSIS ( 4 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
LACERATION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEONATAL DISORDER ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
OSTEOMALACIA ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
POLYDACTYLY ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SKIN HYPERPIGMENTATION ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SKULL MALFORMATION ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
UMBILICAL CORD ABNORMALITY ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
URTICARIA CHRONIC ( 4 FDA reports)
ACANTHOSIS NIGRICANS ( 3 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 3 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOLANGITIS ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FAT REDISTRIBUTION ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HIV PERIPHERAL NEUROPATHY ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTONIA NEONATAL ( 3 FDA reports)
HYPOURICAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MECONIUM STAIN ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PLACENTAL INFARCTION ( 3 FDA reports)
PLEURAL FIBROSIS ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PRENATAL SCREENING TEST ABNORMAL ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RIB FRACTURE ( 3 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKIN SWELLING ( 3 FDA reports)
STOMACH MASS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
THALASSAEMIA ALPHA ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME CONGENITAL ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACHOLIA ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
AIDS RELATED COMPLICATION ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
AMINOACIDURIA ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AMOEBIC DYSENTERY ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOGENITAL WARTS ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BARTHOLIN'S CYST ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CORTISOL ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA FOETAL ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHROMOSOMAL MUTATION ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 2 FDA reports)
CONGENITAL URETHRAL ANOMALY ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
ERYTHEMA NODOSUM ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FIBROSIS ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HIV INFECTION CDC GROUP III ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
INJECTION SITE EROSION ( 2 FDA reports)
INJECTION SITE PUSTULE ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
KERATOSIS PILARIS ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOGLOBINAEMIA ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
TERMINAL INSOMNIA ( 2 FDA reports)
TESTICULAR ATROPHY ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TUBEROUS SCLEROSIS ( 2 FDA reports)
ULCER ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VIRAL LOAD DECREASED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AIDS DEMENTIA COMPLEX ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAL CANCER RECURRENT ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSHIDROSIS ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERGOT POISONING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACTOR II MUTATION ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGUS CSF TEST POSITIVE ( 1 FDA reports)
FUNISITIS ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIV WASTING SYNDROME ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIC RICKETS ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KAPOSI'S SARCOMA AIDS RELATED ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT ANORECTAL NEOPLASM ( 1 FDA reports)
MALIGNANT TUMOUR EXCISION ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITOCHONDRIAL DNA DELETION ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SCHISTOSOMIASIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THORACIC OPERATION ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UMBILICAL ERYTHEMA ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY SEDIMENT ABNORMAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
VAGINITIS GARDNERELLA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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