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
121809523 12180952 3 F 20160119 20160627 20160315 20160711 PER US-PFIZER INC-2016112074 PFIZER 49.00 YR F Y 83.91000 KG 20160711 OT 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
121809523 12180952 1 PS LYRICA PREGABALIN 1 Oral 25MG TWICE DAILY CAPSULE BY MOUTH Y 21446 25 MG CAPSULE, HARD BID
121809523 12180952 2 SS LYRICA PREGABALIN 1 50 MG, UNK Y 21446 50 MG CAPSULE, HARD
121809523 12180952 3 SS LYRICA PREGABALIN 1 75MG TWICE DAILY Y 21446 75 MG CAPSULE, HARD BID
121809523 12180952 4 C TAMOXIFEN TAMOXIFEN 1 Oral 100 MG, DAILY 0 100 MG TABLET
121809523 12180952 5 C TAMOXIFEN TAMOXIFEN 1 20 MG, 1X/DAY 0 20 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121809523 12180952 1 Neuropathy peripheral
121809523 12180952 4 Breast cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121809523 12180952 Fatigue
121809523 12180952 Product use issue
121809523 12180952 Somnolence

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
121809523 12180952 1 20160119 0
121809523 12180952 3 20160208 0
121809523 12180952 5 201104 0