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
125586721 12558672 1 I 20150601 20160715 20160715 PER US-ZYDUS-008389 ZYDUS PHARM 53.00 YR F Y 0.00000 20160714 CN US US

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
125586721 12558672 1 PS WARFARIN WARFARIN 1 Oral UKNOWN 40663 5 MG TABLET QD
125586721 12558672 2 C HYDROCODONE HYDROCODONE 1 U 0
125586721 12558672 3 C ALPRAZOLAM. ALPRAZOLAM 1 U 0
125586721 12558672 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 U 0
125586721 12558672 5 C FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125586721 12558672 1 Coagulopathy
125586721 12558672 2 Product used for unknown indication
125586721 12558672 3 Product used for unknown indication
125586721 12558672 4 Product used for unknown indication
125586721 12558672 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125586721 12558672 Dizziness
125586721 12558672 Lethargy
125586721 12558672 Product odour abnormal
125586721 12558672 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found