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
126104412 12610441 2 F 20150403 20160726 20160801 20160912 EXP FR-009507513-1501FRA007361 MERCK 59.66 YR F Y 59.00000 KG 20160912 CN 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
126104412 12610441 1 PS IMPLANON ETONOGESTREL 1 Subdermal UNK 779308/859235 21529 IMPLANT
126104412 12610441 2 C AOTAL ACAMPROSATE CALCIUM 1 Oral 333MG, 2 TABLETS BID U 0 333 MG TABLET BID
126104412 12610441 3 C TIAPRIDAL TIAPRIDE HYDROCHLORIDE 1 Oral 100MG, 1/2 TABLET BID U 0 TABLET BID
126104412 12610441 4 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 50MG, 1/2 TABLET TID U 0 TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126104412 12610441 1 Contraception
126104412 12610441 2 Depression
126104412 12610441 3 Depression
126104412 12610441 4 Depression

Outcome of event

Event ID CASEID OUTC COD
126104412 12610441 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126104412 12610441 Cervix cautery
126104412 12610441 Complication associated with device
126104412 12610441 Depression
126104412 12610441 Fatigue
126104412 12610441 Incorrect drug administration duration
126104412 12610441 Irritability
126104412 12610441 Nausea
126104412 12610441 Sensation of foreign body
126104412 12610441 Skin infection
126104412 12610441 Vaginal infection
126104412 12610441 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
126104412 12610441 1 20060404 0