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

HYPOTENSION ( 6 FDA reports)
VERTIGO ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FALL ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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