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

DRUG EXPOSURE DURING PREGNANCY ( 19 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLOOD BILIRUBIN INCREASED ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
LIPASE INCREASED ( 9 FDA reports)
VOMITING ( 9 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
MALAISE ( 6 FDA reports)
PAIN ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
FANCONI SYNDROME ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
RASH ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 4 FDA reports)
CHILLS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
THIRST ( 4 FDA reports)
AMNESIA ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
FOETAL CARDIAC DISORDER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEPHROSCLEROSIS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
VASCULAR DEMENTIA ( 3 FDA reports)
ANGER ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 2 FDA reports)
CONGENITAL URINARY TRACT OBSTRUCTION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
POLYDACTYLY ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RHYTHM IDIOVENTRICULAR ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TRISOMY 18 ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD HIV RNA DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHROMOSOMAL DELETION ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL HIV INFECTION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIGEORGE'S SYNDROME ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY OEDEMA NEONATAL ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETROVIRAL INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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