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
102619722 10261972 2 F 20160915 20140626 20160920 PER US-PFIZER INC-2014170926 PFIZER 54.00 YR F Y 0.00000 20160920 MD 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
102619722 10261972 1 PS GABAPENTIN. GABAPENTIN 1 UNK U 20235

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
102619722 10261972 Drug hypersensitivity
102619722 10261972 Peripheral swelling
102619722 10261972 Rash
102619722 10261972 Swelling face

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

no results found

Therapies reported

no results found