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

DYSPNOEA ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERMITTENT CLAUDICATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ASTHMA ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLEEDING ANOVULATORY ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL INCREASED ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL MEGAURETER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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