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

HAEMOPTYSIS ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
SHOCK ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
RASH ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
COUGH ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
RALES ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
STUPOR ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABASIA ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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