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
126056451 12605645 1 I 20160719 20160729 20160729 EXP GB-TEVA-678969ACC TEVA 0.00 M Y 0.00000 20160729 CN GB GB

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
126056451 12605645 1 PS GABAPENTIN. GABAPENTIN 1 Unknown U 76017
126056451 12605645 2 SS GABAPENTIN. GABAPENTIN 1 U 76017
126056451 12605645 3 SS GABAPENTIN. GABAPENTIN 1 U 76017

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126056451 12605645 1 Neuralgia
126056451 12605645 2 Paraesthesia
126056451 12605645 3 Eating disorder

Outcome of event

Event ID CASEID OUTC COD
126056451 12605645 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126056451 12605645 Adverse event
126056451 12605645 General physical health deterioration
126056451 12605645 Insomnia
126056451 12605645 Lung cancer metastatic

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

no results found

Therapies reported

no results found