The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126672891 12667289 1 I 20160809 0 20160818 20160818 DIR 3.36 YR F N 10.50000 KG 20160812 N MD US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126672891 12667289 1 PS DEXAMETHASONE. DEXAMETHASONE 1 0 36 MG
126672891 12667289 2 SS ONCASPAR PEGASPARGASE 1 0 1325 IU
126672891 12667289 3 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 2.4 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126672891 12667289 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126672891 12667289 Agitation
126672891 12667289 Alanine aminotransferase increased
126672891 12667289 Aspartate aminotransferase increased
126672891 12667289 Blood blister
126672891 12667289 Blood glucose decreased
126672891 12667289 Candida infection
126672891 12667289 Cardiac arrest
126672891 12667289 Erythema
126672891 12667289 Hypotension
126672891 12667289 Metabolic acidosis
126672891 12667289 Platelet count decreased
126672891 12667289 Pleural effusion
126672891 12667289 Pseudomonas test positive
126672891 12667289 Pyrexia
126672891 12667289 Rash
126672891 12667289 Respiratory distress
126672891 12667289 Swelling
126672891 12667289 Tachycardia
126672891 12667289 Ulcer
126672891 12667289 Wound

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
126672891 12667289 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126672891 12667289 1 20160809 0
126672891 12667289 2 20160724 0
126672891 12667289 3 20160804 0