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
127173091 12717309 1 I 20160603 20160829 20160906 20160906 EXP CN-GLAXOSMITHKLINE-CN2016GSK128389 GLAXOSMITHKLINE 34.00 YR M Y 55.00000 KG 20160906 OT CN CN

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
127173091 12717309 1 PS DICLOFENAC SODIUM. DICLOFENAC SODIUM 1 Oral 25 MG, TID Y X0985 22122 25 MG FILM-COATED TABLET TID
127173091 12717309 2 SS DICLOFENAC SODIUM. DICLOFENAC SODIUM 1 Y 22122 FILM-COATED TABLET
127173091 12717309 3 SS DICLOFENAC SODIUM. DICLOFENAC SODIUM 1 Y 22122 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127173091 12717309 1 Pyrexia
127173091 12717309 2 Joint swelling
127173091 12717309 3 Pain

Outcome of event

Event ID CASEID OUTC COD
127173091 12717309 OT
127173091 12717309 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127173091 12717309 Laryngeal obstruction
127173091 12717309 Pharyngeal hypoaesthesia
127173091 12717309 Pruritus

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127173091 12717309 1 20160603 20160603 0