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
127014891 12701489 1 I 20160826 20160831 20160831 PER US-PFIZER INC-2016407963 PFIZER 50.00 YR F Y 0.00000 20160831 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
127014891 12701489 1 PS GABAPENTIN. GABAPENTIN 1 UNK U 20235
127014891 12701489 2 SS FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 UNK U 0
127014891 12701489 3 SS OXYBUTYNIN OXYBUTYNIN 1 UNK U 0
127014891 12701489 4 SS PENICILLIN G PENICILLIN G 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127014891 12701489 Drug hypersensitivity

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

no results found

Therapies reported

no results found