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
125706681 12570668 1 I 20160630 20160706 20160719 20160719 PER US-PFIZER INC-2016333864 PFIZER 57.00 YR F Y 68.00000 KG 20160719 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
125706681 12570668 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY 21992 50 MG PROLONGED-RELEASE TABLET QD
125706681 12570668 2 I PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 21992 PROLONGED-RELEASE TABLET
125706681 12570668 3 I DOXYCYCLINE. DOXYCYCLINE 1 Oral 100 MG, 2X/DAY 1000 MG N 0 100 MG CAPSULE BID
125706681 12570668 4 C ASPIRIN /00002701/ ASPIRIN 1 81 MG, 1X/DAY 0 81 MG TABLET QD
125706681 12570668 5 C ALLERTEK 2 10 MG, 1X/DAY 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125706681 12570668 1 Anxiety
125706681 12570668 2 Depression
125706681 12570668 3 Bronchitis
125706681 12570668 4 Cardiac disorder
125706681 12570668 5 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125706681 12570668 Bronchitis
125706681 12570668 Drug interaction
125706681 12570668 Influenza like illness
125706681 12570668 Paraesthesia

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
125706681 12570668 1 2011 0
125706681 12570668 3 20160629 20160703 0