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
119454372 11945437 2 F 2016 20160822 20160125 20160825 EXP BR-PFIZER INC-2016035464 PFIZER 0.00 F Y 0.00000 20160825 CN BR BR

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
119454372 11945437 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 STRENGTH 50MG N Y 21992 PROLONGED-RELEASE TABLET
119454372 11945437 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 STRENGTH 100MG N Y 97693 21992 PROLONGED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119454372 11945437 1 Depression

Outcome of event

Event ID CASEID OUTC COD
119454372 11945437 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119454372 11945437 Anxiety
119454372 11945437 Decreased appetite
119454372 11945437 Depression
119454372 11945437 Disease recurrence
119454372 11945437 Dysentery Dysentery
119454372 11945437 Headache Headache
119454372 11945437 Malaise Malaise
119454372 11945437 Nausea Nausea
119454372 11945437 Retching Retching
119454372 11945437 Salivary hypersecretion Salivary hypersecretion
119454372 11945437 Tearfulness

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
119454372 11945437 1 20160117 201601 0
119454372 11945437 2 2016 2016 0