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
109621198 10962119 8 F 2015 20160831 20150327 20160902 EXP US-PFIZER INC-2015104694 PFIZER 62.00 YR F Y 82.86000 KG 20160902 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
109621198 10962119 1 PS LYRICA PREGABALIN 1 UNK 21446 CAPSULE, HARD
109621198 10962119 2 SS LYRICA PREGABALIN 1 600 MG, 3X/DAY 21446 600 MG CAPSULE, HARD TID
109621198 10962119 3 SS LYRICA PREGABALIN 1 600 MG, 3X/DAY M59942 21446 600 MG CAPSULE, HARD TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109621198 10962119 1 Neuropathy peripheral
109621198 10962119 2 Paraesthesia

Outcome of event

Event ID CASEID OUTC COD
109621198 10962119 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109621198 10962119 Crohn's disease
109621198 10962119 Gait disturbance
109621198 10962119 Intentional product use issue
109621198 10962119 Lymphoedema
109621198 10962119 Malaise
109621198 10962119 Muscle spasms
109621198 10962119 Musculoskeletal discomfort
109621198 10962119 Overdose
109621198 10962119 Pain
109621198 10962119 Pain in extremity
109621198 10962119 Tinnitus

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
109621198 10962119 1 2008 0