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

DRUG EXPOSURE DURING PREGNANCY ( 256 FDA reports)
HYPERTENSION ( 89 FDA reports)
CAESAREAN SECTION ( 86 FDA reports)
PREMATURE BABY ( 70 FDA reports)
NAUSEA ( 58 FDA reports)
BLOOD PRESSURE INCREASED ( 42 FDA reports)
HEADACHE ( 42 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 41 FDA reports)
PRE-ECLAMPSIA ( 41 FDA reports)
VOMITING ( 41 FDA reports)
DYSPNOEA ( 40 FDA reports)
PYREXIA ( 40 FDA reports)
DIZZINESS ( 39 FDA reports)
DIARRHOEA ( 38 FDA reports)
ANAEMIA ( 35 FDA reports)
OEDEMA PERIPHERAL ( 34 FDA reports)
RENAL FAILURE ( 34 FDA reports)
DRUG INEFFECTIVE ( 32 FDA reports)
RENAL IMPAIRMENT ( 32 FDA reports)
PREGNANCY ( 31 FDA reports)
ANXIETY ( 30 FDA reports)
PULMONARY OEDEMA ( 30 FDA reports)
VENTRICULAR HYPERTROPHY ( 30 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 28 FDA reports)
PAIN ( 28 FDA reports)
OLIGOHYDRAMNIOS ( 27 FDA reports)
BLOOD CREATININE INCREASED ( 26 FDA reports)
HYPOTENSION ( 26 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 25 FDA reports)
CARDIOMEGALY ( 25 FDA reports)
INSOMNIA ( 25 FDA reports)
SOMNOLENCE ( 25 FDA reports)
COUGH ( 24 FDA reports)
HAEMOGLOBIN DECREASED ( 23 FDA reports)
MALAISE ( 23 FDA reports)
CONSTIPATION ( 22 FDA reports)
DEPRESSION ( 22 FDA reports)
CONDITION AGGRAVATED ( 21 FDA reports)
LOSS OF CONSCIOUSNESS ( 21 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 20 FDA reports)
CHEST PAIN ( 20 FDA reports)
DEHYDRATION ( 20 FDA reports)
PULMONARY EMBOLISM ( 20 FDA reports)
RENAL FAILURE ACUTE ( 20 FDA reports)
ABORTION SPONTANEOUS ( 19 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
DECREASED APPETITE ( 19 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 19 FDA reports)
MYOCARDIAL INFARCTION ( 19 FDA reports)
CONGENITAL CYTOMEGALOVIRUS INFECTION ( 18 FDA reports)
FATIGUE ( 18 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
HAEMOLYTIC ANAEMIA ( 18 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 18 FDA reports)
PAROTITIS ( 18 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 18 FDA reports)
CARDIAC ARREST ( 17 FDA reports)
FOETAL GROWTH RETARDATION ( 17 FDA reports)
HYPERHIDROSIS ( 17 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 17 FDA reports)
PROTEINURIA ( 17 FDA reports)
RASH ( 17 FDA reports)
ASTHENIA ( 16 FDA reports)
ASTHMA ( 16 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 16 FDA reports)
BRADYCARDIA ( 16 FDA reports)
CEREBROVASCULAR ACCIDENT ( 16 FDA reports)
TACHYCARDIA ( 16 FDA reports)
ARTHRALGIA ( 15 FDA reports)
ATRIAL FIBRILLATION ( 15 FDA reports)
BLOOD UREA INCREASED ( 15 FDA reports)
DIABETES MELLITUS ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
THROMBOSIS ( 15 FDA reports)
CARDIO-RESPIRATORY ARREST ( 14 FDA reports)
CONGENITAL ANOMALY ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
HAEMODIALYSIS ( 14 FDA reports)
INFECTION ( 14 FDA reports)
INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
JOINT SWELLING ( 14 FDA reports)
LIVER DISORDER ( 14 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 14 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
PLATELET COUNT DECREASED ( 14 FDA reports)
WEIGHT INCREASED ( 14 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 13 FDA reports)
CHILLS ( 13 FDA reports)
CHOLELITHIASIS ( 13 FDA reports)
CONFUSIONAL STATE ( 13 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 13 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 13 FDA reports)
JAUNDICE ( 13 FDA reports)
OEDEMA ( 13 FDA reports)
POLYHYDRAMNIOS ( 13 FDA reports)
PREMATURE LABOUR ( 13 FDA reports)
RESTLESSNESS ( 13 FDA reports)
RHABDOMYOLYSIS ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
ABNORMAL LABOUR ( 12 FDA reports)
ABORTION INDUCED ( 12 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 12 FDA reports)
DEATH ( 12 FDA reports)
DEEP VEIN THROMBOSIS ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
FOETAL ARRHYTHMIA ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
PROTEIN URINE PRESENT ( 12 FDA reports)
STAPHYLOCOCCAL INFECTION ( 12 FDA reports)
BACK PAIN ( 11 FDA reports)
CARDIAC MURMUR ( 11 FDA reports)
DYSARTHRIA ( 11 FDA reports)
FACE OEDEMA ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
GESTATIONAL DIABETES ( 11 FDA reports)
HAEMATOCRIT DECREASED ( 11 FDA reports)
HEART DISEASE CONGENITAL ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
JAUNDICE NEONATAL ( 11 FDA reports)
KIDNEY ENLARGEMENT ( 11 FDA reports)
MITRAL VALVE INCOMPETENCE ( 11 FDA reports)
PNEUMONIA ( 11 FDA reports)
RENAL APLASIA ( 11 FDA reports)
SHOCK ( 11 FDA reports)
THREATENED LABOUR ( 11 FDA reports)
WEIGHT DECREASED ( 11 FDA reports)
ARTHRITIS ( 10 FDA reports)
BLOOD IRON DECREASED ( 10 FDA reports)
BLOOD POTASSIUM INCREASED ( 10 FDA reports)
CHEST DISCOMFORT ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
DEAFNESS NEUROSENSORY ( 10 FDA reports)
FOETAL DISTRESS SYNDROME ( 10 FDA reports)
HELLP SYNDROME ( 10 FDA reports)
HEPATIC STEATOSIS ( 10 FDA reports)
NASOPHARYNGITIS ( 10 FDA reports)
NEONATAL DISORDER ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
TREMOR ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ATRIAL SEPTAL DEFECT ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 9 FDA reports)
CRANIOSYNOSTOSIS ( 9 FDA reports)
EMOTIONAL DISTRESS ( 9 FDA reports)
ENCEPHALOPATHY ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
FALL ( 9 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
NEPHROGENIC ANAEMIA ( 9 FDA reports)
OSTEOPOROSIS ( 9 FDA reports)
PALPITATIONS ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
SMALL FOR DATES BABY ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
BREECH PRESENTATION ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CLEFT PALATE ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
DIALYSIS ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
ECLAMPSIA ( 8 FDA reports)
FOETAL DISORDER ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
PREMATURE DELIVERY ( 8 FDA reports)
PULMONARY HYPERTENSION ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SOLITARY KIDNEY ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
APGAR SCORE LOW ( 7 FDA reports)
AZOTAEMIA ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BLOOD URIC ACID INCREASED ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
CLEFT UVULA ( 7 FDA reports)
COLITIS ULCERATIVE ( 7 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 7 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DEVELOPMENTAL DELAY ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DIFFICULTY IN WALKING ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 7 FDA reports)
FIBRIN D DIMER INCREASED ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
HYPOSPADIAS ( 7 FDA reports)
HYPOTONIA NEONATAL ( 7 FDA reports)
IRON DEFICIENCY ANAEMIA ( 7 FDA reports)
NEUROLOGICAL SYMPTOM ( 7 FDA reports)
NORMAL NEWBORN ( 7 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SURGERY ( 7 FDA reports)
UMBILICAL CORD ABNORMALITY ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
VENTRICULAR FIBRILLATION ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
AKATHISIA ( 6 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 6 FDA reports)
ASTHMATIC CRISIS ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DERMATITIS ( 6 FDA reports)
DILATATION ATRIAL ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
FEEDING DISORDER ( 6 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
HAEMORRHAGE ( 6 FDA reports)
HEPATITIS ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
INTRA-UTERINE DEATH ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MULTIPLE ALLERGIES ( 6 FDA reports)
OMPHALITIS ( 6 FDA reports)
PNEUMONIA ASPIRATION ( 6 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
SYSTOLIC HYPERTENSION ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
AMBLYOPIA ( 5 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CEREBELLAR HAEMORRHAGE ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 5 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DELUSION ( 5 FDA reports)
DYSMORPHISM ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
ECONOMIC PROBLEM ( 5 FDA reports)
FEAR ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
GRANULOMA ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPERCHOLESTEROLAEMIA ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOCALCAEMIA ( 5 FDA reports)
INJURY ( 5 FDA reports)
LOGORRHOEA ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
PERITONITIS ( 5 FDA reports)
PHLEBITIS SUPERFICIAL ( 5 FDA reports)
PNEUMONIA HAEMOPHILUS ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RENAL TUBULAR DISORDER ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SLEEP APNOEA SYNDROME ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
STRESS ( 5 FDA reports)
SWELLING ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APNOEA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBRAL HAEMATOMA ( 4 FDA reports)
COARCTATION OF THE AORTA ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DELAYED FONTANELLE CLOSURE ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG INTOLERANCE ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPRAXIA ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
FOETAL HYPOKINESIA ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GESTATIONAL HYPERTENSION ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GLUCOSE URINE PRESENT ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INTESTINAL ULCER ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MITRAL VALVE STENOSIS ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 4 FDA reports)
POSTURE ABNORMAL ( 4 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL DYSPLASIA ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RETCHING ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
TAKAYASU'S ARTERITIS ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
UNIVENTRICULAR HEART ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
UTERINE SPASM ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANAPHYLACTOID SYNDROME OF PREGNANCY ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BODY HEIGHT BELOW NORMAL ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CAUDAL REGRESSION SYNDROME ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
COMA ( 3 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CYANOSIS NEONATAL ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HETEROPHORIA ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYPERMETROPIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
IGA NEPHROPATHY ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INITIAL INSOMNIA ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
MACROSOMIA ( 3 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MITRAL VALVE CALCIFICATION ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
PANCREATIC PSEUDOCYST ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL FAILURE NEONATAL ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RETINOPATHY ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SKULL MALFORMATION ( 3 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
TALIPES ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABO INCOMPATIBILITY ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE PSYCHOSIS ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
AGITATION NEONATAL ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
APLASIA CUTIS CONGENITA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AUTOPHONY ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BILIARY DILATATION ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PROLACTIN INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BONE DEFORMITY ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA NEONATAL ( 2 FDA reports)
BRAIN STEM SYNDROME ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BREECH DELIVERY ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONGENITAL HAND MALFORMATION ( 2 FDA reports)
CONGENITAL INFECTION ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIABETIC COMPLICATION ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FALLOT'S TETRALOGY ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
FOETAL HEART RATE DISORDER ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GRANULOCYTOPENIA NEONATAL ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOTHERMIA NEONATAL ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
IRRITABLE BOWEL SYNDROME ( 2 FDA reports)
LABYRINTHITIS ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICROGNATHIA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MODERATE MENTAL RETARDATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYELOCYTOSIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBSESSIVE THOUGHTS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROTID GLAND ENLARGEMENT ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 2 FDA reports)
PREGNANCY WITH ADVANCED MATERNAL AGE ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRODUCT COMMINGLING ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PUERPERAL PYREXIA ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY MALFORMATION ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STRABISMUS CONGENITAL ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
TREMOR NEONATAL ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENOUS VALVE RUPTURED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTED PREGNANCY ( 1 FDA reports)
ACCESSORY SPLEEN ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL INSUFFICIENCY NEONATAL ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APATHY ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
ARRHYTHMIA NEONATAL ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASTEATOSIS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD INSULIN ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYCARDIA FOETAL ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CITRIC ACID URINE DECREASED ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 1 FDA reports)
CONGENITAL SKIN DISORDER ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
CONGENITAL URETHRAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAGLE BARRETT SYNDROME ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERPHOSPHATURIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
IMMINENT ABORTION ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LATE DEVELOPER ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LE CELLS PRESENT ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE PREGNANCY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEONATAL ANURIA ( 1 FDA reports)
NEONATAL CARDIAC FAILURE ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEONATAL TETANY ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOTHERAPY ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY DISSECTION ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPTH DECREASED ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
RUBELLA IN PREGNANCY ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THANATOPHORIC DWARFISM ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETHRAL VALVES ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE HAEMATOMA ( 1 FDA reports)
UTERINE POLYPECTOMY ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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