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
126000381 12600038 1 I 201512 20160721 20160727 20160727 EXP SE-MPA-2016-004318 SE-PFIZER INC-2016356071 PFIZER 0.00 M Y 0.00000 20160727 CN SE SE

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
126000381 12600038 1 PS NEURONTIN GABAPENTIN 1 100 MG, DAILY 20235 100 MG
126000381 12600038 2 SS NEURONTIN GABAPENTIN 1 1800 MG, DAILY 20235 1800 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126000381 12600038 1 Fibromyalgia
126000381 12600038 2 Pain

Outcome of event

Event ID CASEID OUTC COD
126000381 12600038 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126000381 12600038 Anxiety
126000381 12600038 Depressed mood
126000381 12600038 Depression
126000381 12600038 Derealisation
126000381 12600038 Diarrhoea
126000381 12600038 Disturbance in attention
126000381 12600038 Fatigue
126000381 12600038 Product use issue
126000381 12600038 Suicidal ideation

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
126000381 12600038 1 201512 0