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
123049113 12304911 3 F 2010 20160614 20160426 20160707 PER US-PFIZER INC-2016188834 PFIZER 57.00 YR F Y 0.00000 20160707 MD 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
123049113 12304911 1 PS GABAPENTIN. GABAPENTIN 1 UNK 20235
123049113 12304911 2 SS GABAPENTIN. GABAPENTIN 1 600 MG, 2X/DAY 20235 600 MG BID
123049113 12304911 3 SS GABAPENTIN. GABAPENTIN 1 1200 MG, 1X/DAY NIGHTLY 20235 1200 MG QD
123049113 12304911 4 C DICLOFENAC DICLOFENAC 1 75 MG, 2X/DAY 0 75 MG BID
123049113 12304911 5 C ROBAXIN METHOCARBAMOL 1 500 MG, 3X/DAY 0 500 MG TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123049113 12304911 1 Fibromyalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123049113 12304911 Drug ineffective for unapproved indication

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
123049113 12304911 2 20160308 0
123049113 12304911 5 201604 0