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
127462111 12746211 1 I 20160826 20160907 20160915 20160915 EXP GB-ABBVIE-16P-167-1728723-00 ABBVIE 19.00 YR F Y 60.00000 KG 20160915 CN GB GB

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
127462111 12746211 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Oral 500 MG Y UNKNOWN 50698

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127462111 12746211 1 Ear infection bacterial

Outcome of event

Event ID CASEID OUTC COD
127462111 12746211 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127462111 12746211 Anxiety
127462111 12746211 Crying
127462111 12746211 Nightmare

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
127462111 12746211 1 20160826 20160828 0