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
127456161 12745616 1 I 20150601 0 20160914 20160914 DIR FDA-CTU 59.00 YR F N 126.00000 LBS 20160709 Y 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
127456161 12745616 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral 1 PILL N D 0 1 DF PILLULES QD
127456161 12745616 3 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 0
127456161 12745616 5 C ELAVIL AMITRIPTYLINE HYDROCHLORIDE 1 0
127456161 12745616 7 C ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 0
127456161 12745616 9 C REGLAN METOCLOPRAMIDE HYDROCHLORIDE 1 0
127456161 12745616 11 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 0
127456161 12745616 13 C ESTRACE ESTRADIOL 1 0
127456161 12745616 15 C LUNESTA ESZOPICLONE 1 0
127456161 12745616 17 C CALCIUM CALCIUM 1 0
127456161 12745616 19 C TUMS CALCIUM CARBONATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127456161 12745616 1 Anxiety
127456161 12745616 1 Depression

Outcome of event

Event ID CASEID OUTC COD
127456161 12745616 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127456161 12745616 Activities of daily living impaired
127456161 12745616 Dizziness
127456161 12745616 Drug ineffective
127456161 12745616 Migraine
127456161 12745616 Nausea
127456161 12745616 Withdrawal syndrome

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
127456161 12745616 1 20071120 20150820 0