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
125546691 12554669 1 I 20160307 20160706 20160713 20160713 EXP FR-BAUSCH-BL-2016-016818 BAUSCH AND LOMB 88.00 YR F Y 0.00000 20160713 OT FR FR

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
125546691 12554669 1 SS TRIATEC RAMIPRIL 1 Oral Y 0 1.25 MG CAPSULE QD
125546691 12554669 2 PS ZOVIRAX ACYCLOVIR 1 Intravenous (not otherwise specified) U 18604 500 G INJECTION TID
125546691 12554669 3 SS CLAMOXYL AMOXICILLINCLAVULANIC ACID 1 Intravenous (not otherwise specified) Y 0 4 G INJECTION TID
125546691 12554669 4 SS NORSET MIRTAZAPINE 1 Oral U 0 15 MG FILM-COATED TABLET QD
125546691 12554669 5 SS OPTIRAY IOVERSOL 1 Intravenous (not otherwise specified) 0 350 MG INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125546691 12554669 1 Product used for unknown indication
125546691 12554669 2 Encephalitis
125546691 12554669 3 Encephalitis
125546691 12554669 4 Product used for unknown indication
125546691 12554669 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125546691 12554669 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125546691 12554669 Acute kidney injury
125546691 12554669 Haematuria

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
125546691 12554669 1 20160307 0
125546691 12554669 2 20160226 20160307 0
125546691 12554669 3 20160226 20160307 0
125546691 12554669 4 20160226 20160307 0
125546691 12554669 5 20160301 20160302 0