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
126370944 12637094 4 F 201401 20160822 20160809 20160902 EXP US-TEVA-681693USA TEVA 23.04 YR F Y 52.16000 KG 20160902 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
126370944 12637094 1 PS PROVIGIL MODAFINIL 1 50-100 MG 20717 QD
126370944 12637094 2 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 10 MILLIGRAM DAILY; 0 10 MG QD
126370944 12637094 3 C PRENATAL VITAMINS VITAMINS 1 0 QD
126370944 12637094 4 C VITAMIN B6 PYRIDOXINE HYDROCHLORIDE 1 0
126370944 12637094 5 C CALCIUM CALCIUM 1 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126370944 12637094 1 Fatigue
126370944 12637094 2 Hypersensitivity
126370944 12637094 3 Pregnancy
126370944 12637094 4 Vitamin supplementation
126370944 12637094 5 Vitamin supplementation

Outcome of event

Event ID CASEID OUTC COD
126370944 12637094 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126370944 12637094 Abortion spontaneous
126370944 12637094 Exposure during pregnancy
126370944 12637094 Off label use

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
126370944 12637094 1 201401 20160514 0
126370944 12637094 2 2010 20160613 0
126370944 12637094 3 20160519 0
126370944 12637094 4 20160530 0
126370944 12637094 5 2010 0