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
126827311 12682731 1 I 20160616 20160811 20160825 20160825 EXP GB-MHRA-ADR 23591721 GB-TEVA-685528ACC TEVA 16.00 YR Y 0.00000 20160825 OT 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
126827311 12682731 1 PS HALOPERIDOL. HALOPERIDOL 1 U U 71617

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126827311 12682731 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126827311 12682731 Dysphagia
126827311 12682731 Swollen tongue

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
126827311 12682731 1 20160616 0