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
124887492 12488749 2 F 2016 20160819 20160622 20160824 EXP US-PFIZER INC-2016309499 PFIZER 22.00 YR F Y 70.00000 KG 20160824 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
124887492 12488749 1 PS GABAPENTIN. GABAPENTIN 1 600 MG, 3X/DAY 20235 600 MG CAPSULE, HARD TID
124887492 12488749 2 SS GABAPENTIN. GABAPENTIN 1 600 MG, 3X/DAY 20235 600 MG CAPSULE, HARD TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124887492 12488749 1 Migraine
124887492 12488749 2 Muscle twitching

Outcome of event

Event ID CASEID OUTC COD
124887492 12488749 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124887492 12488749 Drug detoxification
124887492 12488749 Dyskinesia
124887492 12488749 Generalised tonic-clonic seizure
124887492 12488749 Product use issue

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
124887492 12488749 1 20160101 201605 0