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
127283181 12728318 1 I 0 20160907 20160907 DIR US-FDA-349973 FDA-CTU 74.00 YR F N 66.15000 KG 20160907 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
127283181 12728318 1 PS SERTRALINE HCL SERTRALINE HYDROCHLORIDE 1 Oral N D 20170308 0 90 DF COATED TABLET QD
127283181 12728318 2 C SIMVASTATIN. SIMVASTATIN 1 0
127283181 12728318 3 C VERAPAMIL ER VERAPAMIL HYDROCHLORIDE 1 0
127283181 12728318 4 C LORSARTAN HCTZ 2 0
127283181 12728318 5 C LORAZEPAM. LORAZEPAM 1 0
127283181 12728318 6 C CENTRUM SILVER- WOMEN 50+ 2 0
127283181 12728318 7 C WALGREENS GLUCOSAMINE CHONDROITIN MSM + VITAMIN D3 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127283181 12728318 1 Depression

Outcome of event

Event ID CASEID OUTC COD
127283181 12728318 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127283181 12728318 Depression
127283181 12728318 Drug ineffective
127283181 12728318 Product substitution issue

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found