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
126620621 12662062 1 I 20160718 20160805 20160817 20160817 EXP PT-PRESTIUM-2016RN000346 RENAISSANCE 0.00 Y 0.00000 20160817 OT PT PT

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
126620621 12662062 1 PS ZOVIRAX ACYCLOVIR 1 Oral 200 MG, DAILY N 2Y2G 20089 200 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126620621 12662062 1 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126620621 12662062 OT
126620621 12662062 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126620621 12662062 Decreased appetite
126620621 12662062 Delirium
126620621 12662062 Diet refusal
126620621 12662062 Generalised erythema
126620621 12662062 Generalised oedema
126620621 12662062 Hypotension
126620621 12662062 Pyrexia
126620621 12662062 Rash generalised
126620621 12662062 Respiratory distress
126620621 12662062 Throat irritation

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
126620621 12662062 1 20160715 20160726 0