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
106837574 10683757 4 F 20160824 20141230 20160830 PER US-PFIZER INC-2014357483 PFIZER 65.00 YR F Y 83.91000 KG 20160830 PH US BR

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
106837574 10683757 1 PS LYRICA PREGABALIN 1 Oral 50 MG, 3X/DAY 21446 50 MG CAPSULE, HARD TID
106837574 10683757 2 SS LYRICA PREGABALIN 1 100 MG, 3X/DAY 21446 100 MG CAPSULE, HARD TID
106837574 10683757 3 SS GABAPENTIN. GABAPENTIN 1 300 MG, 2X/DAY U 20235 300 MG CAPSULE, HARD BID
106837574 10683757 4 SS GABAPENTIN. GABAPENTIN 1 300 MG, 3X/DAY U 20235 300 MG CAPSULE, HARD TID
106837574 10683757 5 SS NEURONTIN GABAPENTIN 1 Oral 300 MG, 2X/DAY 20235 300 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106837574 10683757 1 Neuropathy peripheral
106837574 10683757 2 Pain
106837574 10683757 3 Neuropathy peripheral
106837574 10683757 4 Pain
106837574 10683757 5 Diabetic neuropathy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
106837574 10683757 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
106837574 10683757 5 20141118 0