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
125267921 12526792 1 I 20160618 20160620 20160705 20160705 PER US-PFIZER INC-2016309872 PFIZER 55.00 YR M Y 81.65000 KG 20160705 CN US 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
125267921 12526792 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, DAILY Y 21992 50 MG PROLONGED-RELEASE TABLET
125267921 12526792 2 SS GLUTEN WHEAT GLUTEN 1 UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125267921 12526792 1 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125267921 12526792 Agitation
125267921 12526792 Blood pressure increased
125267921 12526792 Erythema
125267921 12526792 Expired product administered
125267921 12526792 Feeling hot
125267921 12526792 Irritability
125267921 12526792 Pruritus
125267921 12526792 Urticaria

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125267921 12526792 1 20160617 20160617 0