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

SUICIDE ATTEMPT ( 9 FDA reports)
PRURITUS ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
PNEUMONIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ACNE ( 6 FDA reports)
AFFECT LABILITY ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PARONYCHIA ( 6 FDA reports)
PNEUMONITIS ( 6 FDA reports)
SEBORRHOEIC DERMATITIS ( 6 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
DEPRESSIVE SYMPTOM ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
BRONCHITIS ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
COUGH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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