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
127603501 12760350 1 I 20160913 20160919 20160919 EXP US-PFIZER INC-2016433849 PFIZER 52.00 YR M Y 111.13000 KG 20160919 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
127603501 12760350 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY (ONCE AT NIGHT TIME) N67728 21992 50 MG PROLONGED-RELEASE TABLET QD
127603501 12760350 2 C TRIAZOLAM. TRIAZOLAM 1 Oral 0.25 MG, 3X/DAY THREE TIMES AT NIGHT 0 .25 MG TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127603501 12760350 1 Depression
127603501 12760350 2 Insomnia

Outcome of event

Event ID CASEID OUTC COD
127603501 12760350 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127603501 12760350 Dysuria
127603501 12760350 Urinary retention
127603501 12760350 Urine output decreased

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
127603501 12760350 1 20160721 0
127603501 12760350 2 1986 0