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
126762251 12676225 1 I 20160701 20160823 20160823 PER US-PFIZER INC-2016330026 PFIZER 60.00 YR F Y 0.00000 20160823 OT 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
126762251 12676225 1 PS SKELAXIN METAXALONE 1 Oral 800 MG, 3X/DAY 13217 800 MG TABLET TID
126762251 12676225 2 SS SKELAXIN METAXALONE 1 Oral 800 MG, AS NEEDED (TID) 13217 800 MG TABLET
126762251 12676225 3 SS SKELAXIN METAXALONE 1 13217 TABLET
126762251 12676225 4 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral 10 MG, AS NEEDED (ONCE A DAY ) 0 10 MG TABLET
126762251 12676225 5 C DICLOFENAC POTASSIUM. DICLOFENAC POTASSIUM 1 Oral 50 MG, AS NEEDED (TWICE DAILY) 0 50 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126762251 12676225 1 Muscle spasms
126762251 12676225 2 Myalgia
126762251 12676225 3 Back pain
126762251 12676225 5 Back pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126762251 12676225 Drug hypersensitivity

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
126762251 12676225 2 20160229 20160810 0