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
125788071 12578807 1 I 2014 20160715 20160721 20160721 EXP AU-EISAI MEDICAL RESEARCH-EC-2016-018744 EISAI 0.00 M Y 0.00000 20160721 CN AU AU

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
125788071 12578807 1 PS PARIET RABEPRAZOLE SODIUM 1 Oral UNKNOWN Y 20973 TABLET
125788071 12578807 2 C ASPIRIN. ASPIRIN 1 Unknown UNKNOWN 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125788071 12578807 1 Product used for unknown indication
125788071 12578807 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125788071 12578807 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125788071 12578807 Chest pain
125788071 12578807 Cough
125788071 12578807 Insomnia
125788071 12578807 Muscular weakness
125788071 12578807 Oropharyngeal pain
125788071 12578807 Palpitations
125788071 12578807 Rhinorrhoea

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
125788071 12578807 1 201411 20160711 0