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
127746051 12774605 1 I 2016 20160805 20160923 20160923 PER US-MYLANLABS-2016M1033402 MYLAN 0.00 F Y 62.59000 KG 20160923 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
127746051 12774605 1 PS CELECOXIB. CELECOXIB 1 Oral 200 MG, QD 3076569 78857 200 MG CAPSULE QD
127746051 12774605 2 C ASPIRIN /00002701/ ASPIRIN 1 UNK D 0
127746051 12774605 3 C LYRICA PREGABALIN 1 UNK D 0
127746051 12774605 4 C TAMOXIFEN TAMOXIFEN 1 UNK D 0
127746051 12774605 5 C PROZAC FLUOXETINE HYDROCHLORIDE 1 UNK D 0
127746051 12774605 6 C SKELAXIN METAXALONE 1 UNK D 0
127746051 12774605 7 C VESICARE SOLIFENACIN SUCCINATE 1 UNK, QD D 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127746051 12774605 1 Musculoskeletal discomfort

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127746051 12774605 Drug effect decreased
127746051 12774605 Pain

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
127746051 12774605 1 201607 0