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
125618081 12561808 1 I 20160712 20160715 20160715 EXP US-PFIZER INC-2016343745 PFIZER 0.00 F Y 0.00000 20160715 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
125618081 12561808 1 PS ZOLOFT SERTRALINE HYDROCHLORIDE 1 UNK N 19839
125618081 12561808 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 UNK U 21992 PROLONGED-RELEASE TABLET
125618081 12561808 3 SS PAXIL PAROXETINE HYDROCHLORIDE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125618081 12561808 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125618081 12561808 Gastric infection
125618081 12561808 Gastrointestinal disorder
125618081 12561808 Malaise
125618081 12561808 Nausea
125618081 12561808 Vomiting

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
125618081 12561808 2 201602 0