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

DRUG INTERACTION ( 169 FDA reports)
PREGNANCY ( 136 FDA reports)
DIARRHOEA ( 114 FDA reports)
NAUSEA ( 108 FDA reports)
RENAL FAILURE ACUTE ( 108 FDA reports)
BLOOD BILIRUBIN INCREASED ( 105 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 101 FDA reports)
PYREXIA ( 97 FDA reports)
JAUNDICE ( 92 FDA reports)
HYPERBILIRUBINAEMIA ( 91 FDA reports)
VOMITING ( 87 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 73 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 71 FDA reports)
RASH ( 70 FDA reports)
CAESAREAN SECTION ( 69 FDA reports)
ABORTION SPONTANEOUS ( 67 FDA reports)
HEADACHE ( 66 FDA reports)
ANAEMIA ( 65 FDA reports)
RENAL FAILURE ( 62 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 60 FDA reports)
PNEUMONIA ( 59 FDA reports)
WEIGHT DECREASED ( 57 FDA reports)
NORMAL NEWBORN ( 56 FDA reports)
NEPHROLITHIASIS ( 54 FDA reports)
ASTHENIA ( 53 FDA reports)
BLOOD CREATININE INCREASED ( 51 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 51 FDA reports)
ABDOMINAL PAIN ( 50 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 50 FDA reports)
RHABDOMYOLYSIS ( 47 FDA reports)
MALAISE ( 43 FDA reports)
DYSPNOEA ( 42 FDA reports)
FATIGUE ( 42 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 42 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 41 FDA reports)
CUSHING'S SYNDROME ( 39 FDA reports)
HYPERLIPIDAEMIA ( 39 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 36 FDA reports)
THROMBOCYTOPENIA ( 36 FDA reports)
LIPODYSTROPHY ACQUIRED ( 33 FDA reports)
MYALGIA ( 32 FDA reports)
NEUROPATHY PERIPHERAL ( 32 FDA reports)
DECREASED APPETITE ( 31 FDA reports)
DEPRESSION ( 31 FDA reports)
DIZZINESS ( 30 FDA reports)
HEPATITIS ( 30 FDA reports)
MYOCARDIAL INFARCTION ( 30 FDA reports)
OCULAR ICTERUS ( 30 FDA reports)
PANCREATITIS ( 30 FDA reports)
PREMATURE BABY ( 30 FDA reports)
RENAL TUBULAR NECROSIS ( 30 FDA reports)
SEPSIS ( 30 FDA reports)
PRURITUS ( 28 FDA reports)
RENAL IMPAIRMENT ( 27 FDA reports)
DIABETES MELLITUS ( 26 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 26 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 26 FDA reports)
OSTEONECROSIS ( 26 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 26 FDA reports)
CONDITION AGGRAVATED ( 25 FDA reports)
CONGENITAL TERATOMA ( 25 FDA reports)
DEHYDRATION ( 25 FDA reports)
DRUG INEFFECTIVE ( 25 FDA reports)
HAEMATURIA ( 25 FDA reports)
HEPATIC STEATOSIS ( 25 FDA reports)
RENAL TUBULAR DISORDER ( 25 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 24 FDA reports)
HEPATITIS C ( 24 FDA reports)
HYPOKALAEMIA ( 24 FDA reports)
INSOMNIA ( 24 FDA reports)
OVERDOSE ( 24 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 23 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 23 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 23 FDA reports)
HYPOTENSION ( 23 FDA reports)
PROTEINURIA ( 23 FDA reports)
ARTHRALGIA ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 22 FDA reports)
HEPATIC ENZYME INCREASED ( 22 FDA reports)
LIVER DISORDER ( 22 FDA reports)
PAIN ( 22 FDA reports)
PANCYTOPENIA ( 22 FDA reports)
ABORTION INDUCED ( 21 FDA reports)
ADRENAL SUPPRESSION ( 21 FDA reports)
ARRHYTHMIA ( 21 FDA reports)
BACK PAIN ( 21 FDA reports)
CHOLESTASIS ( 21 FDA reports)
COUGH ( 21 FDA reports)
DRUG HYPERSENSITIVITY ( 21 FDA reports)
HYPOPHOSPHATAEMIA ( 21 FDA reports)
LACTIC ACIDOSIS ( 21 FDA reports)
OEDEMA PERIPHERAL ( 21 FDA reports)
PLATELET COUNT DECREASED ( 21 FDA reports)
RENAL COLIC ( 21 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 21 FDA reports)
FANCONI SYNDROME ACQUIRED ( 20 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 20 FDA reports)
SUBDURAL HAEMATOMA ( 20 FDA reports)
CONVULSION ( 19 FDA reports)
DEATH ( 19 FDA reports)
GAIT DISTURBANCE ( 19 FDA reports)
HEPATIC FAILURE ( 19 FDA reports)
HEPATITIS B ( 19 FDA reports)
RESPIRATORY DISTRESS ( 19 FDA reports)
TREMOR ( 19 FDA reports)
HEPATIC CIRRHOSIS ( 18 FDA reports)
HYPERSENSITIVITY ( 18 FDA reports)
HYPERTENSION ( 18 FDA reports)
PARAESTHESIA ( 18 FDA reports)
STILLBIRTH ( 18 FDA reports)
BLOOD GLUCOSE INCREASED ( 17 FDA reports)
CEREBROVASCULAR ACCIDENT ( 17 FDA reports)
HAEMOLYTIC ANAEMIA ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
LIPOATROPHY ( 17 FDA reports)
METABOLIC ACIDOSIS ( 17 FDA reports)
MYOSITIS ( 17 FDA reports)
PARKINSONISM ( 17 FDA reports)
RASH MACULO-PAPULAR ( 17 FDA reports)
SOMNOLENCE ( 17 FDA reports)
TRANSAMINASES INCREASED ( 17 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 17 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 17 FDA reports)
ANOREXIA ( 16 FDA reports)
LEUKOPENIA ( 16 FDA reports)
MYOCLONUS ( 16 FDA reports)
NEPHROPATHY TOXIC ( 16 FDA reports)
PAIN IN EXTREMITY ( 16 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 16 FDA reports)
POLYDACTYLY ( 16 FDA reports)
RESPIRATORY FAILURE ( 16 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 15 FDA reports)
CHEST PAIN ( 15 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 15 FDA reports)
LIVE BIRTH ( 15 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 15 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 14 FDA reports)
DRUG LEVEL INCREASED ( 14 FDA reports)
DRUG RESISTANCE ( 14 FDA reports)
DRY SKIN ( 14 FDA reports)
KAPOSI'S SARCOMA ( 14 FDA reports)
MULTI-ORGAN FAILURE ( 14 FDA reports)
ORAL CANDIDIASIS ( 14 FDA reports)
PLEURAL EFFUSION ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
ADRENAL INSUFFICIENCY ( 13 FDA reports)
CHILLS ( 13 FDA reports)
CHROMATURIA ( 13 FDA reports)
CONFUSIONAL STATE ( 13 FDA reports)
CRYPTORCHISM ( 13 FDA reports)
DRUG TOXICITY ( 13 FDA reports)
HERPES SIMPLEX ( 13 FDA reports)
HYPONATRAEMIA ( 13 FDA reports)
INFECTION ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
NEUTROPENIA ( 13 FDA reports)
PALPITATIONS ( 13 FDA reports)
CACHEXIA ( 12 FDA reports)
DYSPHAGIA ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
HYPERCHOLESTEROLAEMIA ( 12 FDA reports)
INCORRECT DOSE ADMINISTERED ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 12 FDA reports)
NEPHRITIS ( 12 FDA reports)
NEPHRITIS INTERSTITIAL ( 12 FDA reports)
OSTEOPOROSIS ( 12 FDA reports)
SUICIDAL IDEATION ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
AIDS ENCEPHALOPATHY ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 11 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 11 FDA reports)
CELL DEATH ( 11 FDA reports)
COMA ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
HODGKIN'S DISEASE ( 11 FDA reports)
HYDROCEPHALUS ( 11 FDA reports)
HYPERLACTACIDAEMIA ( 11 FDA reports)
HYPOAESTHESIA ( 11 FDA reports)
LYMPHOMA ( 11 FDA reports)
NERVOUS SYSTEM DISORDER ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
PANCREATITIS ACUTE ( 11 FDA reports)
POLYNEUROPATHY ( 11 FDA reports)
PREMATURE LABOUR ( 11 FDA reports)
SMALL FOR DATES BABY ( 11 FDA reports)
SWELLING FACE ( 11 FDA reports)
VENTRICULAR FIBRILLATION ( 11 FDA reports)
VIRAL LOAD INCREASED ( 11 FDA reports)
ABDOMINAL DISTENSION ( 10 FDA reports)
ACUTE ABDOMEN ( 10 FDA reports)
ANXIETY ( 10 FDA reports)
ASCITES ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
DRUG INTOLERANCE ( 10 FDA reports)
FANCONI SYNDROME ( 10 FDA reports)
GALLBLADDER DISORDER ( 10 FDA reports)
HEPATOTOXICITY ( 10 FDA reports)
HYPOGLYCAEMIA ( 10 FDA reports)
INFLUENZA LIKE ILLNESS ( 10 FDA reports)
LIVER INJURY ( 10 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 10 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 10 FDA reports)
MEDICATION ERROR ( 10 FDA reports)
MELAENA ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
PULMONARY HYPERTENSION ( 10 FDA reports)
PULMONARY TUBERCULOSIS ( 10 FDA reports)
SKIN INFECTION ( 10 FDA reports)
TREATMENT NONCOMPLIANCE ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 9 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
BLOOD URIC ACID INCREASED ( 9 FDA reports)
CALCULUS URINARY ( 9 FDA reports)
CERVICAL INCOMPETENCE ( 9 FDA reports)
CHOLECYSTITIS ( 9 FDA reports)
CONGENITAL ANOMALY ( 9 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 9 FDA reports)
CYTOLYTIC HEPATITIS ( 9 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 9 FDA reports)
DILATATION ATRIAL ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 9 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 9 FDA reports)
ENCEPHALITIS VIRAL ( 9 FDA reports)
FACIAL PARESIS ( 9 FDA reports)
GLYCOSURIA ( 9 FDA reports)
HEPATOSPLENOMEGALY ( 9 FDA reports)
HIV INFECTION ( 9 FDA reports)
MOBILITY DECREASED ( 9 FDA reports)
MUSCLE SPASMS ( 9 FDA reports)
NECK PAIN ( 9 FDA reports)
OPTIC NEURITIS ( 9 FDA reports)
PSORIASIS ( 9 FDA reports)
SPLENOMEGALY ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
VERTIGO ( 9 FDA reports)
AFFECT LABILITY ( 8 FDA reports)
APPENDICITIS ( 8 FDA reports)
BLISTER ( 8 FDA reports)
BLOOD LACTIC ACID INCREASED ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CONDUCTION DISORDER ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
ERECTILE DYSFUNCTION ( 8 FDA reports)
FACIAL WASTING ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
GLAUCOMA ( 8 FDA reports)
HEPATITIS ACUTE ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 8 FDA reports)
NEPHROPATHY ( 8 FDA reports)
NEPHROTIC SYNDROME ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
OSTEOPENIA ( 8 FDA reports)
PREMATURE DELIVERY ( 8 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 8 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
TORSADE DE POINTES ( 8 FDA reports)
VIROLOGIC FAILURE ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD AMYLASE INCREASED ( 7 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 7 FDA reports)
BLOOD CORTISOL DECREASED ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
COLITIS ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 7 FDA reports)
ENCEPHALOPATHY ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 7 FDA reports)
FACE OEDEMA ( 7 FDA reports)
GASTRITIS ( 7 FDA reports)
HAEMANGIOMA ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 7 FDA reports)
MITOCHONDRIAL TOXICITY ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
MYASTHENIA GRAVIS ( 7 FDA reports)
POLYURIA ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
PRE-ECLAMPSIA ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SINUS TACHYCARDIA ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ACIDOSIS ( 6 FDA reports)
AORTIC ANEURYSM RUPTURE ( 6 FDA reports)
BASEDOW'S DISEASE ( 6 FDA reports)
BILE DUCT STONE ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CHORIOAMNIONITIS ( 6 FDA reports)
CLEFT PALATE ( 6 FDA reports)
DIGEORGE'S SYNDROME ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FALLOT'S TETRALOGY ( 6 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
GASTROENTERITIS SHIGELLA ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
INJECTION SITE PAIN ( 6 FDA reports)
IRON DEFICIENCY ANAEMIA ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LIPOHYPERTROPHY ( 6 FDA reports)
LUNG NEOPLASM MALIGNANT ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
NIGHTMARE ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PURPURA ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SUDDEN CARDIAC DEATH ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
TRISOMY 21 ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
UVEITIS ( 6 FDA reports)
VASCULITIS ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
ABNORMAL DREAMS ( 5 FDA reports)
ABORTION THREATENED ( 5 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 5 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 5 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
APLASIA ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
BALANCE DISORDER ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CLEFT LIP AND PALATE ( 5 FDA reports)
CONGENITAL JAW MALFORMATION ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
CRYSTAL NEPHROPATHY ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DYSLIPIDAEMIA ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
ENTEROBACTER SEPSIS ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
FALL ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
GOITRE ( 5 FDA reports)
HAEMATOMA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 5 FDA reports)
HYDROPS FOETALIS ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
JAUNDICE NEONATAL ( 5 FDA reports)
KIDNEY SMALL ( 5 FDA reports)
LIMB MALFORMATION ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NEPHROCALCINOSIS ( 5 FDA reports)
NEURALGIA ( 5 FDA reports)
NEUROTOXICITY ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OSTEOMYELITIS ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
SYNDACTYLY ( 5 FDA reports)
TALIPES ( 5 FDA reports)
TEARFULNESS ( 5 FDA reports)
THIRST ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
TWIN PREGNANCY ( 5 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 5 FDA reports)
UNINTENDED PREGNANCY ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VANISHING BILE DUCT SYNDROME ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ACUTE HIV INFECTION ( 4 FDA reports)
AGITATION ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
APPENDICITIS PERFORATED ( 4 FDA reports)
ASEPTIC NECROSIS BONE ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
CALCULUS URETERIC ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBROVASCULAR DISORDER ( 4 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ECLAMPSIA ( 4 FDA reports)
ECTOPIC PREGNANCY ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GROIN ABSCESS ( 4 FDA reports)
GUILLAIN-BARRE SYNDROME ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HIV PERIPHERAL NEUROPATHY ( 4 FDA reports)
HIV WASTING SYNDROME ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
IMMUNODEFICIENCY ( 4 FDA reports)
INJECTION SITE PRURITUS ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
KLINEFELTER'S SYNDROME ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LIPIDS ABNORMAL ( 4 FDA reports)
LOSS OF LIBIDO ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MALARIA ( 4 FDA reports)
MASS ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MYELITIS ( 4 FDA reports)
NEONATAL DISORDER ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PERIOSTITIS ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
POLYSUBSTANCE ABUSE ( 4 FDA reports)
PORENCEPHALY ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RENAL NECROSIS ( 4 FDA reports)
SECONDARY SYPHILIS ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRISOMY 18 ( 4 FDA reports)
TUMOUR RUPTURE ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VASCULITIS NECROTISING ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
VIITH NERVE PARALYSIS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ACUTE SINUSITIS ( 3 FDA reports)
ADRENAL ADENOMA ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AMNIOCENTESIS ABNORMAL ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
B-CELL LYMPHOMA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD HIV RNA INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BREECH PRESENTATION ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 3 FDA reports)
CHRONIC HEPATIC FAILURE ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CSF GLUCOSE ABNORMAL ( 3 FDA reports)
CSF PROTEIN INCREASED ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
ERGOT POISONING ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FOETAL CARDIAC DISORDER ( 3 FDA reports)
FOETAL GROWTH RETARDATION ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HAEMATOMA EVACUATION ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERPARATHYROIDISM ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INGUINAL HERNIA ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
KIDNEY FIBROSIS ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIVER CARCINOMA RUPTURED ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 3 FDA reports)
MUSCLE INJURY ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEUROSYPHILIS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PARANOID PERSONALITY DISORDER ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PLATELET DISORDER ( 3 FDA reports)
PLATELET TOXICITY ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKELETAL INJURY ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TERATOMA ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TONSILLITIS ( 3 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 3 FDA reports)
TRISOMY 15 ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VIRAL LOAD DECREASED ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
AMNIOCENTESIS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
CAPUT MEDUSAE ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC ENZYMES ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CENTRAL OBESITY ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CONGENITAL HEPATOMEGALY ( 2 FDA reports)
CONGENITAL TORTICOLLIS ( 2 FDA reports)
CONGENITAL URINARY TRACT OBSTRUCTION ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
CORNEAL ULCER ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
CUPULOLITHIASIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ECZEMA NUMMULAR ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
FAT ATROPHY ( 2 FDA reports)
FAT REDISTRIBUTION ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HIV ASSOCIATED NEPHROPATHY ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYDROCHOLECYSTIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOPHONESIS ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
INADEQUATE DIET ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGEAL PAIN ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPH NODE PAIN ( 2 FDA reports)
LYMPHADENITIS BACTERIAL ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
MICROALBUMINURIA ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PERITONEAL FIBROSIS ( 2 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 2 FDA reports)
RETROVIRAL INFECTION ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SALIVARY GLAND CALCULUS ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SELECTIVE ABORTION ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN NEOPLASM EXCISION ( 2 FDA reports)
SKULL MALFORMATION ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
SUPERINFECTION LUNG ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THYROXINE FREE DECREASED ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
UTERINE CANCER ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VIRAL MUTATION IDENTIFIED ( 2 FDA reports)
VISION ABNORMAL NEONATAL ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 2 FDA reports)
WOLF-HIRSCHHORN SYNDROME ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABNORMAL PRODUCT OF CONCEPTION ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AIDS DEMENTIA COMPLEX ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMINOACIDURIA ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY NEGATIVE ( 1 FDA reports)
ANTIRETROVIRAL THERAPY ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BARTTER'S SYNDROME ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE ABNORMAL ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ERYTHROPOIETIN ABNORMAL ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHORDEE ( 1 FDA reports)
CHROMOSOMAL DELETION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CONGENITAL GENITAL MALFORMATION MALE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
END STAGE AIDS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLOTTIS CARCINOMA ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPALLAESTHESIA ( 1 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL MASS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE CARDIAC DEFECTS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEMATODIASIS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE II ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANCREATOGENOUS DIABETES ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOBIA OF FLYING ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PROCTITIS HERPES ( 1 FDA reports)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA ( 1 FDA reports)
PROPHYLAXIS AGAINST TRANSPLANT REJECTION ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PSEUDOCYST ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RICKETTSIOSIS ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TAKAYASU'S ARTERITIS ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONSILLITIS BACTERIAL ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC RUPTURE ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
VIBRATORY SENSE INCREASED ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME CONGENITAL ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
XEROSIS ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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