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
126994832 12699483 2 F 20160813 20160829 20160830 20160901 PER US-PFIZER INC-2016409221 PFIZER 55.00 YR F Y 57.00000 KG 20160901 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
126994832 12699483 1 PS SULFASALAZINE. SULFASALAZINE 1 Oral 500 MG, 2X/DAY 6000 MG Y 7073 500 MG TABLET BID
126994832 12699483 2 C FOLIC ACID. FOLIC ACID 1 Oral 1 MG, DAILY 0 1 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126994832 12699483 1 Rheumatoid arthritis
126994832 12699483 2 Arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126994832 12699483 Aphasia
126994832 12699483 Asthenia
126994832 12699483 Chest discomfort
126994832 12699483 Chills
126994832 12699483 Decreased appetite
126994832 12699483 Dizziness
126994832 12699483 Dyspnoea
126994832 12699483 Headache
126994832 12699483 Influenza like illness
126994832 12699483 Nasopharyngitis
126994832 12699483 Nausea

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
126994832 12699483 1 20160812 20160826 0
126994832 12699483 2 20160705 20160826 0