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

DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
METRORRHAGIA ( 4 FDA reports)
CARTILAGE INJURY ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
RASH ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
FALL ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SYNOVIAL CYST ( 2 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUPUS ENDOCARDITIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAINFLUENZAE VIRAL LARYNGOTRACHEOBRONCHITIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URINOMA ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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