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
127328571 12732857 1 I 20160909 0 20160910 20160910 DIR US-FDA-350304 FDA-CTU 29.00 YR F N 65.25000 KG 20160910 N 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
127328571 12732857 1 PS AMBIEN ZOLPIDEM TARTRATE 1 Oral Y D 20170909 0 2 DF COATED TABLET HS
127328571 12732857 3 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 0
127328571 12732857 5 C YASMIN DROSPIRENONEETHINYL ESTRADIOL 1 0
127328571 12732857 7 C SOOLANTRA IVERMECTIN 1 0
127328571 12732857 9 C ATIVAN LORAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127328571 12732857 1 Insomnia

Outcome of event

Event ID CASEID OUTC COD
127328571 12732857 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127328571 12732857 Drug effect increased
127328571 12732857 Hallucination
127328571 12732857 Hypersomnia
127328571 12732857 Paranoia
127328571 12732857 Product substitution issue
127328571 12732857 Somnolence
127328571 12732857 Suicidal ideation

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
127328571 12732857 1 20160909 20160910 0