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
106557623 10655762 3 F 201501 20160719 20141216 20160726 PER US-PFIZER INC-2014341488 PFIZER 64.00 YR F Y 146.00000 KG 20160726 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
106557623 10655762 1 PS LYRICA PREGABALIN 1 75 MG, 3X/DAY 21446 75 MG TID
106557623 10655762 2 SS LYRICA PREGABALIN 1 75 MG, 3X/DAY M83431 21446 75 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106557623 10655762 1 Fibromyalgia
106557623 10655762 2 Neuropathy peripheral

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
106557623 10655762 Feeling abnormal
106557623 10655762 Feeling jittery
106557623 10655762 Nervousness

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
106557623 10655762 1 2013 0
106557623 10655762 2 2012 0