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

DYSPNOEA ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FALL ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SMEAR SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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