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

DRUG EXPOSURE DURING PREGNANCY ( 87 FDA reports)
NEUTROPENIA ( 41 FDA reports)
ANAEMIA ( 30 FDA reports)
PREMATURE BABY ( 25 FDA reports)
VOMITING ( 23 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 22 FDA reports)
PREGNANCY ( 22 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
PNEUMONIA ( 19 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
JOINT DISLOCATION ( 18 FDA reports)
WEIGHT DECREASED ( 18 FDA reports)
DIARRHOEA ( 17 FDA reports)
HYPOTENSION ( 17 FDA reports)
NAUSEA ( 17 FDA reports)
HEADACHE ( 16 FDA reports)
DEATH ( 14 FDA reports)
DIZZINESS ( 14 FDA reports)
PREMATURE LABOUR ( 14 FDA reports)
PYREXIA ( 14 FDA reports)
AGITATION ( 13 FDA reports)
CONVULSION ( 13 FDA reports)
POLYDACTYLY ( 13 FDA reports)
CAESAREAN SECTION ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
TORSADE DE POINTES ( 12 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 12 FDA reports)
BLOOD MAGNESIUM DECREASED ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
DYSKINESIA ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
ATAXIA ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
HEPATOMEGALY ( 10 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
COUGH ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
NEONATAL DISORDER ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
VENTRICULAR ARRHYTHMIA ( 9 FDA reports)
BACK PAIN ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
DEVELOPMENTAL DELAY ( 8 FDA reports)
HYDROCELE ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
SMALL FOR DATES BABY ( 8 FDA reports)
ABORTION SPONTANEOUS ( 7 FDA reports)
ANAEMIA MACROCYTIC ( 7 FDA reports)
ANXIETY ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
BLOOD BICARBONATE DECREASED ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
CARDIOPULMONARY FAILURE ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
METABOLIC ACIDOSIS ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
PAIN ( 7 FDA reports)
POOR SUCKING REFLEX ( 7 FDA reports)
RASH ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SEPSIS NEONATAL ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
UMBILICAL HERNIA ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
ABORTION INDUCED ( 6 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
COMPLEX PARTIAL SEIZURES ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
DRUG LEVEL INCREASED ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HEPATOSPLENOMEGALY ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
HYPOSPADIAS ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
MACROCYTOSIS ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
ADVERSE EVENT ( 5 FDA reports)
ALBUMINURIA ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
CEREBRAL ARTERY STENOSIS ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FACTOR VIII INHIBITION ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
INFLUENZA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
NORMAL NEWBORN ( 5 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ANAEMIA NEONATAL ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
CYSTIC FIBROSIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
GENE MUTATION ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
JAUNDICE NEONATAL ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NEUROMYOPATHY ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RETROPERITONEAL NEOPLASM ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
TRISOMY 21 ( 4 FDA reports)
TWIN PREGNANCY ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABORTION THREATENED ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BREECH PRESENTATION ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONGENITAL NAEVUS ( 3 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 3 FDA reports)
CONGENITAL TOXOPLASMOSIS ( 3 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 3 FDA reports)
CRYING ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CYST ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GIARDIASIS ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HIV INFECTION ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERLACTACIDAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INJECTION SITE REACTION ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIPODYSTROPHY ACQUIRED ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MICROCEPHALY ( 3 FDA reports)
MICROGNATHIA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENTRICULAR HYPOPLASIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION NEONATAL ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLIGHTED OVUM ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BREECH DELIVERY ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOANAL ATRESIA ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CONGENITAL HEPATOMEGALY ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DEPENDENCE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSTROPHIA MYOTONICA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FOETAL ARRHYTHMIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HIV ANTIBODY POSITIVE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMAN ANTI-MOUSE ANTIBODY POSITIVE ( 2 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 2 FDA reports)
HUMAN IMMUNODEFICIENCY VIRUS TRANSMISSION ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPENIA NEONATAL ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHLEBITIS SUPERFICIAL ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
SCAB ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TRISOMY 18 ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UTERINE INVERSION ( 2 FDA reports)
VARICOPHLEBITIS ( 2 FDA reports)
VASCULITIS CEREBRAL ( 2 FDA reports)
VIRAL TEST POSITIVE ( 2 FDA reports)
VIROLOGIC FAILURE ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASIA CUTIS CONGENITA ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLAST CELLS ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATARACT CONGENITAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CLEFT UVULA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DUODENAL ATRESIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
EPISPADIAS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
FALL ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FREE FATTY ACIDS INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KAPOSI'S SARCOMA AIDS RELATED ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALIGNANT DYSPHAGIA ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
OBESITY ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHORTENED CERVIX ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SOLITARY KIDNEY ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRISOMY 17 ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL LOAD ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)

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