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
125261592 12526159 2 F 201509 20160727 20160705 20160810 PER US-PFIZER INC-2016312154 PFIZER 60.00 YR M Y 0.00000 20160810 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
125261592 12526159 1 PS NEURONTIN GABAPENTIN 1 Oral 100 MG, 3X/DAY Y 20235 100 MG CAPSULE, HARD TID
125261592 12526159 2 SS NEURONTIN GABAPENTIN 1 Oral 100 MG, 4X/DAY Y 20235 100 MG CAPSULE, HARD QID
125261592 12526159 3 SS GRALISE GABAPENTIN 1 300 MG, 1X/DAY Y 0 300 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125261592 12526159 1 Nerve injury
125261592 12526159 3 Nerve injury

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125261592 12526159 Anger
125261592 12526159 Feeling abnormal
125261592 12526159 Irritability
125261592 12526159 Product use issue

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
125261592 12526159 2 20150909 20160505 0
125261592 12526159 3 20160516 20160701 0