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
125800541 12580054 1 I 20160708 20160721 20160721 EXP ES-PERRIGO-16ES018058 PERRIGO 28.00 YR M Y 0.00000 20160721 MD ES ES

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
125800541 12580054 1 PS IBUPROFEN. IBUPROFEN 1 Oral UNK Y UNKNOWN 72096 TABLET
125800541 12580054 2 SS IBUPROFEN. IBUPROFEN 1 Oral 600 MG CUMULATIVE Y UNKNOWN 72096 TABLET
125800541 12580054 3 SS NAPROXEN SODIUM. NAPROXEN SODIUM 1 Oral UNK U U UNKNOWN 0 TABLET
125800541 12580054 4 SS DIPYRONE DIPYRONE 1 Unknown UNK U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125800541 12580054 1 Product used for unknown indication
125800541 12580054 2 Drug provocation test
125800541 12580054 3 Product used for unknown indication
125800541 12580054 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125800541 12580054 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125800541 12580054 Angioedema

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

no results found

Therapies reported

no results found