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
126974623 12697462 3 F 20160815 20160908 20160830 20160915 PER US-PFIZER INC-2016407141 PFIZER 76.00 YR F Y 57.14000 KG 20160915 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
126974623 12697462 1 PS GABAPENTIN. GABAPENTIN 1 UNK 20882 FILM-COATED TABLET
126974623 12697462 2 SS GABAPENTIN. GABAPENTIN 1 Oral 1200 MG, 3X/DAY 20882 1200 MG FILM-COATED TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126974623 12697462 1 Neuropathy peripheral

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126974623 12697462 Chills
126974623 12697462 Diarrhoea
126974623 12697462 Drug ineffective for unapproved indication

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

no results found

Therapies reported

no results found