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
126341591 12634159 1 I 20160718 20160805 20160809 20160809 EXP PT-INFARMED-L201607-245 PT-GLAXOSMITHKLINE-PT2016114169 GLAXOSMITHKLINE 30.19 YR F Y 52.00000 KG 20160809 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
126341591 12634159 1 PS ZOVIRAX ACYCLOVIR 1 Oral VALIDADE: 2021 1800 MG N 2Y2G 18603 200 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126341591 12634159 1 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126341591 12634159 HO
126341591 12634159 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126341591 12634159 Decreased appetite
126341591 12634159 Delirium
126341591 12634159 Diet refusal
126341591 12634159 Generalised erythema
126341591 12634159 Generalised oedema
126341591 12634159 Hypotension
126341591 12634159 Pyrexia
126341591 12634159 Rash generalised
126341591 12634159 Respiratory distress
126341591 12634159 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
126341591 12634159 1 20160715 20160726 0