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
126222981 12622298 1 I 20160215 20160802 20160804 20160804 EXP GB-GLAXOSMITHKLINE-GB2016111828 GLAXOSMITHKLINE 81.00 YR F Y 0.00000 20160804 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
126222981 12622298 1 PS ACYCLOVIR. ACYCLOVIR 1 Unknown UNK U UNCONFIRMED 18603 TABLET
126222981 12622298 2 C RAMIPRIL. RAMIPRIL 1 Unknown 2.5 MG, DAILY U 0 2.5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126222981 12622298 1 Herpes zoster
126222981 12622298 2 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
126222981 12622298 HO
126222981 12622298 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126222981 12622298 Dyspnoea exertional
126222981 12622298 Faeces discoloured
126222981 12622298 Fatigue
126222981 12622298 Pallor
126222981 12622298 Small intestinal haemorrhage

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
126222981 12622298 1 20160204 0