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
123568424 12356842 4 F 20160502 20160718 20160511 20160804 PER US-PFIZER INC-2016223300 PFIZER 45.00 YR F Y 0.00000 20160804 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
123568424 12356842 1 PS GABAPENTIN. GABAPENTIN 1 100 MG, 3X/DAY 20235 100 MG TID
123568424 12356842 2 SS GABAPENTIN. GABAPENTIN 1 100 MG, 3X/DAY 20235 100 MG TID
123568424 12356842 3 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 UNK(ACETAMINOPHEN 325 MG AND OXYCODONE 10 MG) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123568424 12356842 1 Neuralgia
123568424 12356842 2 Sciatica

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123568424 12356842 Activities of daily living impaired
123568424 12356842 Dizziness
123568424 12356842 Drug ineffective for unapproved indication
123568424 12356842 Somnolence

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
123568424 12356842 1 20160414 0
123568424 12356842 2 20160502 0
123568424 12356842 3 1997 0