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
125477773 12547777 3 F 20160515 20160825 20160712 20160906 PER US-009507513-1607USA003001 MERCK 20.54 YR F Y 124.26000 KG 20160906 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
125477773 12547777 1 PS NUVARING ETHINYL ESTRADIOLETONOGESTREL 1 Vaginal 1 DF, 3 WEEKS IN 1 WEEK OUT 1 DF Y 21187 1 DF VAGINAL RING /month
125477773 12547777 2 C CAMBIA DICLOFENAC POTASSIUM 1 U 0
125477773 12547777 3 C ZOMIG ZOLMITRIPTAN 1 U 0
125477773 12547777 4 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 U 0
125477773 12547777 5 C TRAZODONE HYDROCHLORIDE. TRAZODONE HYDROCHLORIDE 1 Oral U 0 TABLET
125477773 12547777 6 C ZOCOR SIMVASTATIN 1 Oral U 0 TABLET
125477773 12547777 7 C AMLODIPINE AMLODIPINE BESYLATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125477773 12547777 1 Contraception

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125477773 12547777 Menorrhagia

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
125477773 12547777 1 201603 20160515 0