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
126478721 12647872 1 I 20160804 20160812 20160812 EXP US-PFIZER INC-2016375939 PFIZER 0.00 F Y 0.00000 20160812 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
126478721 12647872 1 PS SODIUM BICARBONATE. SODIUM BICARBONATE 1 UNK U 77394
126478721 12647872 2 SS ACETYLSALICYLIC ACID ASPIRIN 1 UNK U 0
126478721 12647872 3 SS CITRIC ACID CITRIC ACID MONOHYDRATE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126478721 12647872 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126478721 12647872 Anaphylactic reaction
126478721 12647872 Angioedema
126478721 12647872 Drug hypersensitivity
126478721 12647872 Drug intolerance

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

no results found

Therapies reported

no results found