The Safety Rates Drug Report

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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
122811552 12281155 2 F 2013 20160620 20160419 20160712 PER US-PFIZER INC-2016178720 PFIZER 40.00 YR F Y 91.00000 KG 20160712 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
122811552 12281155 1 PS NEURONTIN GABAPENTIN 1 UNK Y 20235
122811552 12281155 2 SS NEURONTIN GABAPENTIN 1 Y 20235
122811552 12281155 3 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 60 MG, 2X/DAY 0 60 MG BID
122811552 12281155 4 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0
122811552 12281155 5 C SEROQUEL QUETIAPINE FUMARATE 1 50 MG, 1X/DAY AT NIGHT 0 50 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122811552 12281155 1 Pain
122811552 12281155 2 Nerve injury
122811552 12281155 3 Pain
122811552 12281155 4 Depression
122811552 12281155 5 Sleep disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122811552 12281155 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
122811552 12281155 3 2009 0
122811552 12281155 5 201510 0