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
112441323 11244132 3 F 2014 20160912 20150707 20160919 PER US-PFIZER INC-2015221823 PFIZER 55.00 YR F Y 0.00000 20160919 MD 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
112441323 11244132 1 PS GABAPENTIN. GABAPENTIN 1 Oral UNK Y 20235
112441323 11244132 2 SS GABAPENTIN. GABAPENTIN 1 Y 20235
112441323 11244132 3 SS GABAPENTIN. GABAPENTIN 1 Y 20235

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112441323 11244132 1 Pain
112441323 11244132 2 CREST syndrome
112441323 11244132 3 Post herpetic neuralgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
112441323 11244132 Drug hypersensitivity
112441323 11244132 Hypoaesthesia
112441323 11244132 Paraesthesia

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

no results found

Therapies reported

no results found