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
124937755 12493775 5 F 2016 20160826 20160623 20160830 PER US-PFIZER INC-2016291233 PFIZER 61.00 YR F Y 79.38000 KG 20160830 MD 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
124937755 12493775 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY M51570 21992 50 MG PROLONGED-RELEASE TABLET QD
124937755 12493775 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY M51573 21992 50 MG PROLONGED-RELEASE TABLET QD
124937755 12493775 3 C XANAX ALPRAZOLAM 1 0.5 MG, 3X/DAY 0 .5 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124937755 12493775 1 Depression
124937755 12493775 2 Anxiety
124937755 12493775 3 Sleep disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124937755 12493775 Dizziness
124937755 12493775 Drug ineffective
124937755 12493775 Feeling abnormal
124937755 12493775 Incorrect product storage
124937755 12493775 Irritability
124937755 12493775 Nausea
124937755 12493775 Product quality issue

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
124937755 12493775 1 2006 0