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
96043792 9604379 2 F 20160801 20131008 20160812 EXP CA-RANBAXY-2013US-73916 RANBAXY 69.00 YR M Y 0.00000 20160812 PH CA CA

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
96043792 9604379 1 PS GABAPENTIN. GABAPENTIN 1 Unknown 1500 MG, DAILY Y 76606 1500 MG
96043792 9604379 2 SS GABAPENTIN. GABAPENTIN 1 Unknown 300 MG, QD 76606 300 MG
96043792 9604379 3 SS GABAPENTIN. GABAPENTIN 1 Unknown 300 MG, BID 76606 300 MG Q12H
96043792 9604379 4 SS GABAPENTIN. GABAPENTIN 1 Unknown 300 MG, TID 76606 300 MG Q8H
96043792 9604379 5 C PRIMIDONE. PRIMIDONE 1 Unknown 375 MG, DAILY U 0 375 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96043792 9604379 1 Essential tremor
96043792 9604379 2 Essential tremor
96043792 9604379 5 Essential tremor

Outcome of event

Event ID CASEID OUTC COD
96043792 9604379 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
96043792 9604379 Myasthenia gravis
96043792 9604379 Off label use

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

no results found

Therapies reported

no results found