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
100681392 10068139 2 F 20150623 20140409 20150630 EXP US-PFIZER INC-2014094471 PFIZER 0.00 F Y 0.00000 20150630 N 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
100681392 10068139 1 PS LYRICA PREGABALIN 1 UNK D 21446
100681392 10068139 2 SS LYRICA PREGABALIN 1 D 21446
100681392 10068139 3 SS LYRICA PREGABALIN 1 D 21446

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100681392 10068139 1 Post herpetic neuralgia
100681392 10068139 2 Pain
100681392 10068139 3 Herpes zoster

Outcome of event

Event ID CASEID OUTC COD
100681392 10068139 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100681392 10068139 Cataract
100681392 10068139 Condition aggravated
100681392 10068139 Drug effect incomplete
100681392 10068139 Eye disorder
100681392 10068139 Vision blurred

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found