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
123543874 12354387 4 F 201603 20160714 20160511 20160715 EXP DE-009507513-1605GBR004072 MERCK 19.00 YR F Y 0.00000 20160715 CN DE 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
123543874 12354387 1 PS IMPLANON ETONOGESTREL 1 Subcutaneous UNK 21529 IMPLANT
123543874 12354387 2 SS CERAZETTE DESOGESTREL 1 Oral UNK Y 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123543874 12354387 1 Contraception
123543874 12354387 2 Menorrhagia

Outcome of event

Event ID CASEID OUTC COD
123543874 12354387 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123543874 12354387 Dizziness
123543874 12354387 Headache
123543874 12354387 Hypoaesthesia
123543874 12354387 Menorrhagia
123543874 12354387 Nausea
123543874 12354387 Product use issue
123543874 12354387 Visual impairment
123543874 12354387 Vomiting

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
123543874 12354387 1 20160225 0
123543874 12354387 2 20160418 20160506 0