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
126412611 12641261 1 I 201605 20160727 20160810 20160810 PER US-PFIZER INC-2016364428 PFIZER 54.00 YR M Y 97.00000 KG 20160810 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
126412611 12641261 1 PS GABAPENTIN. GABAPENTIN 1 Oral 600 MG, 2X/DAY 20882 600 MG FILM-COATED TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126412611 12641261 1 Diabetic neuropathy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126412611 12641261 Drug ineffective for unapproved indication
126412611 12641261 Eating disorder
126412611 12641261 Gait disturbance
126412611 12641261 Pain in extremity
126412611 12641261 Pre-existing condition improved
126412611 12641261 Therapeutic response unexpected
126412611 12641261 Weight decreased

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

no results found

Therapies reported

no results found