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
1199386713 11993867 13 F 20101026 20160817 20160203 20160825 PER US-009507513-1601USA011133 MERCK 0.00 F Y 68.03000 KG 20160825 MD 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
1199386713 11993867 1 PS IMPLANON ETONOGESTREL 1 Subdermal UNK 21529 IMPLANT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1199386713 11993867 1 Contraception

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
1199386713 11993867 Arthralgia
1199386713 11993867 Chest pain
1199386713 11993867 Complication associated with device
1199386713 11993867 Dizziness
1199386713 11993867 Hypoaesthesia
1199386713 11993867 Incorrect drug administration duration
1199386713 11993867 Joint swelling
1199386713 11993867 Migraine
1199386713 11993867 Ovarian cyst
1199386713 11993867 Pyrexia
1199386713 11993867 Scar

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
1199386713 11993867 1 20101026 0