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
126746381 12674638 1 I 20160811 20160822 20160822 EXP GB-MHRA-ADR 23590668 GB-BAUSCH-BL-2016-020036 BAUSCH AND LOMB 69.00 YR F Y 0.00000 20160822 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
126746381 12674638 1 PS ADIZEM DILTIAZEM HYDROCHLORIDE 1 Unknown U 18602
126746381 12674638 2 SS RAMIPRIL. RAMIPRIL 1 Unknown U 0
126746381 12674638 3 SS LOSARTAN. LOSARTAN 1 Unknown 0
126746381 12674638 4 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126746381 12674638 1 Product used for unknown indication
126746381 12674638 2 Product used for unknown indication
126746381 12674638 3 Product used for unknown indication
126746381 12674638 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126746381 12674638 HO
126746381 12674638 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126746381 12674638 Aphonia
126746381 12674638 Hypokalaemia
126746381 12674638 Pneumonia
126746381 12674638 Syncope

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
126746381 12674638 2 201607 0
126746381 12674638 4 201607 0