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
125632041 12563204 1 I 20160709 20160715 20160715 PER US-PFIZER INC-2016338649 PFIZER 0.00 M Y 0.00000 20160715 CN 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
125632041 12563204 1 PS GABAPENTIN. GABAPENTIN 1 100 MG, 3X/DAY U 20235 100 MG CAPSULE, HARD TID
125632041 12563204 2 SS OXYCODONE AND ACETAMINOPHEN ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 [OXYCODONE HYDROCHLORIDE, 10MG]/[PARACETAMOL, 325 MG] 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125632041 12563204 1 Neuralgia
125632041 12563204 2 Pain

Outcome of event

Event ID CASEID OUTC COD
125632041 12563204 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125632041 12563204 Back pain
125632041 12563204 Feeling abnormal
125632041 12563204 Insomnia
125632041 12563204 Malaise
125632041 12563204 Muscle twitching
125632041 12563204 Myalgia
125632041 12563204 Nerve injury
125632041 12563204 Product use issue
125632041 12563204 Restlessness
125632041 12563204 Tremor

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found