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
124071952 12407195 2 F 20160617 20160526 20160712 PER US-PFIZER INC-2016245352 PFIZER 0.00 F Y 0.00000 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
124071952 12407195 1 PS GABAPENTIN. GABAPENTIN 1 100 MG, 3X/DAY 20235 100 MG TID
124071952 12407195 2 SS GABAPENTIN. GABAPENTIN 1 20235
124071952 12407195 3 SS GABAPENTIN. GABAPENTIN 1 20235
124071952 12407195 4 SS GABAPENTIN. GABAPENTIN 1 20235
124071952 12407195 5 SS GABAPENTIN. GABAPENTIN 1 20235
124071952 12407195 6 SS GABAPENTIN. GABAPENTIN 1 20235

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124071952 12407195 1 Fibromyalgia
124071952 12407195 2 Neck pain
124071952 12407195 3 Musculoskeletal pain
124071952 12407195 4 Pain in extremity
124071952 12407195 5 Pain
124071952 12407195 6 Arthropathy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124071952 12407195 Drug ineffective for unapproved indication
124071952 12407195 Intentional product misuse
124071952 12407195 Pain
124071952 12407195 Sleep disorder

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

no results found

Therapies reported

no results found