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

DUODENAL ULCER ( 50 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 50 FDA reports)
CEREBRAL HAEMORRHAGE ( 36 FDA reports)
NEUTROPENIA ( 26 FDA reports)
HYPONATRAEMIA ( 21 FDA reports)
ANAEMIA ( 20 FDA reports)
DIARRHOEA ( 20 FDA reports)
PNEUMONIA FUNGAL ( 19 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 18 FDA reports)
DEPRESSED MOOD ( 18 FDA reports)
HYPERBILIRUBINAEMIA ( 18 FDA reports)
JAUNDICE ( 18 FDA reports)
OSTEOPOROSIS ( 18 FDA reports)
PNEUMOTHORAX ( 18 FDA reports)
SHOCK ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
PNEUMONIA ( 12 FDA reports)
DELIRIUM ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
AIDS ENCEPHALOPATHY ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 9 FDA reports)
LABORATORY TEST ABNORMAL ( 9 FDA reports)
DEATH ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
CUSHING'S SYNDROME ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
DRUG TOXICITY ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ANAL FISSURE ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
NEURODERMATITIS ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PROCTALGIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGER ( 2 FDA reports)
ASCITES ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HOMICIDAL IDEATION ( 2 FDA reports)
HYDROPNEUMOTHORAX ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PATHOLOGICAL GAMBLING ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
STARVATION ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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