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

DRUG EXPOSURE DURING PREGNANCY ( 18 FDA reports)
RASH ( 17 FDA reports)
NEPHROLITHIASIS ( 16 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 15 FDA reports)
ASTHENIA ( 14 FDA reports)
HYPERSENSITIVITY ( 14 FDA reports)
PYREXIA ( 14 FDA reports)
RASH MACULO-PAPULAR ( 14 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
ABORTION INDUCED ( 10 FDA reports)
ABORTION SPONTANEOUS ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
ANGIOEDEMA ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 9 FDA reports)
EOSINOPHILIA ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
RENAL COLIC ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CYTOLYTIC HEPATITIS ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HIV INFECTION ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
PHLEBITIS ( 6 FDA reports)
PHOTOSENSITIVITY REACTION ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
POLYURIA ( 6 FDA reports)
PREGNANCY ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
VIRAL LOAD INCREASED ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 5 FDA reports)
COUGH ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
OROPHARYNGEAL PAIN ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
VOMITING ( 5 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
CARDIAC MALPOSITION ( 4 FDA reports)
CONGENITAL HEPATOBILIARY ANOMALY ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEFORMITY THORAX ( 4 FDA reports)
DIAPHRAGMATIC APLASIA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
EXOMPHALOS ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HEPATIC DISPLACEMENT ( 4 FDA reports)
HYPOSPADIAS ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
PLACENTA PRAEVIA ( 4 FDA reports)
PLACENTAL INSUFFICIENCY ( 4 FDA reports)
PREMATURE LABOUR ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
THIRST ( 4 FDA reports)
UTERINE HAEMATOMA ( 4 FDA reports)
VAGINAL HAEMORRHAGE ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOETAL GROWTH RESTRICTION ( 3 FDA reports)
FOETAL HEART RATE DISORDER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERPARATHYROIDISM ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LIPODYSTROPHY ACQUIRED ( 3 FDA reports)
MICROENCEPHALY ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NEONATAL ANOXIA ( 3 FDA reports)
NEONATAL INFECTION ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SYNOVITIS ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BOWEN'S DISEASE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 2 FDA reports)
ENLARGED CLITORIS ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENITAL EROSION ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BURSA CALCIFICATION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COMA ( 1 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC ANOMALY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOSALPINX ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCHROMIC ANAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SPASTIC PARAPLEGIA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOPHLEBITIS NEONATAL ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRIFASCICULAR BLOCK ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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