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
127130471 12713047 1 I 20150428 20160822 20160902 20160902 EXP US-PFIZER INC-2016411777 PFIZER 60.00 YR F Y 0.00000 20160902 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
127130471 12713047 1 SS ENBREL ETANERCEPT 1 Unknown UNK UNK, EVERY 3 WEEKS U 1065295 0 SOLUTION FOR INJECTION IN PRE-FILLED PEN
127130471 12713047 2 PS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Unknown UNK U 50711 FILM-COATED TABLET
127130471 12713047 3 C VITAMIN D3 CHOLECALCIFEROL 1 Unknown 2000 IU, UNK 0 2000 IU
127130471 12713047 4 C CALCIUM CALCIUM 1 1200 MG, UNK 0 1200 MG
127130471 12713047 5 C VALACICLOVIR VALACYCLOVIR HYDROCHLORIDE 1 Oral 1 MG, 3X/DAY 0 1 MG TID
127130471 12713047 6 C PREDNISONE. PREDNISONE 1 6 DAY TAPER 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127130471 12713047 1 Rheumatoid arthritis
127130471 12713047 2 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
127130471 12713047 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127130471 12713047 Drug hypersensitivity
127130471 12713047 Facial paralysis
127130471 12713047 Head discomfort
127130471 12713047 Intentional product misuse
127130471 12713047 Pain
127130471 12713047 Rash erythematous
127130471 12713047 Sinusitis

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
127130471 12713047 1 20150428 0