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
123945173 12394517 3 F 2013 20160710 20160523 20160713 PER US-PFIZER INC-2016236469 PFIZER 57.00 YR F Y 77.11000 KG 20160713 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
123945173 12394517 1 PS GABAPENTIN. GABAPENTIN 1 UNK 20235 CAPSULE, HARD
123945173 12394517 2 SS GABAPENTIN. GABAPENTIN 1 400 MG, 3X/DAY 20235 400 MG CAPSULE, HARD TID
123945173 12394517 3 SS GABAPENTIN. GABAPENTIN 1 1200 MG, DAILY 20235 1200 MG CAPSULE, HARD
123945173 12394517 4 C XARELTO RIVAROXABAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123945173 12394517 1 Pain
123945173 12394517 4 Cardiac fibrillation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123945173 12394517 Abdominal pain upper
123945173 12394517 Condition aggravated
123945173 12394517 Dizziness
123945173 12394517 Drug ineffective for unapproved indication
123945173 12394517 Herpes zoster
123945173 12394517 Intentional product misuse
123945173 12394517 Intentional product use issue
123945173 12394517 Musculoskeletal chest pain
123945173 12394517 Pain
123945173 12394517 Pelvic pain

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
123945173 12394517 1 2013 0
123945173 12394517 4 2013 2013 0