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
119486065 11948606 5 F 2011 20160804 20160125 20160809 PER US-BAYER-2016-011952 BAYER 31.00 YR A F Y 68.27000 KG 20160809 OT 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
119486065 11948606 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 82205A 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
119486065 11948606 2 C VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 60 MG, UNK 0 60 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119486065 11948606 1 Contraception
119486065 11948606 2 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
119486065 11948606 HO
119486065 11948606 OT
119486065 11948606 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119486065 11948606 Abdominal pain
119486065 11948606 Abortion spontaneous
119486065 11948606 Anxiety
119486065 11948606 Depression
119486065 11948606 Device issue
119486065 11948606 Drug ineffective
119486065 11948606 Infection
119486065 11948606 Pregnancy with contraceptive device
119486065 11948606 Uterine perforation

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
119486065 11948606 1 20090220 20140312 0
119486065 11948606 2 2011 0