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
124681012 12468101 2 F 2010 20160705 20160615 20160711 EXP US-PFIZER INC-2016293667 PFIZER 58.00 YR M Y 113.40000 KG 20160711 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
124681012 12468101 1 PS NEURONTIN GABAPENTIN 1 Oral 30 MG, 2X/DAY Y 20235 30 MG CAPSULE, HARD BID
124681012 12468101 2 C OXYCODONE OXYCODONE 1 UNK 0
124681012 12468101 3 C ALLOPURINOL. ALLOPURINOL 1 UNK 0
124681012 12468101 4 C NOVOLOG INSULIN ASPART 1 UNK 0
124681012 12468101 5 C VICTOZA LIRAGLUTIDE 1 1.8 UNITS GIVEN IN THE STOMACH NIGHTLY 0 1.8 IU

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124681012 12468101 1 Neuropathy peripheral
124681012 12468101 2 Nephrolithiasis
124681012 12468101 3 Renal disorder
124681012 12468101 4 Diabetes mellitus
124681012 12468101 5 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124681012 12468101 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124681012 12468101 Feeling abnormal
124681012 12468101 Loss of consciousness
124681012 12468101 Product use issue
124681012 12468101 Somnolence

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
124681012 12468101 1 2010 0
124681012 12468101 2 1988 0
124681012 12468101 3 2011 0
124681012 12468101 5 2014 0