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
126615672 12661567 2 F 20160801 20160914 20160817 20160919 PER US-PFIZER INC-2016379925 PFIZER 88.00 YR F Y 45.36000 KG 20160919 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
126615672 12661567 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 11 MG, 1X/DAY N30256 203214 11 MG TABLET QD
126615672 12661567 2 SS PREDNISONE. PREDNISONE 1 UNK U 0
126615672 12661567 3 C AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 Oral UNK, 1X/DAY (5-20 MG) 0 QD
126615672 12661567 4 C LEVOTHYROXIN LEVOTHYROXINE 1 Oral 25 UG, DAILY (AN HOUR BEFORE BREAKFAST) 0 25 UG
126615672 12661567 5 C FISH OIL FISH OIL 1 UNK 0
126615672 12661567 6 C PRESERVISION MINERALSVITAMINS 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126615672 12661567 1 Arthritis
126615672 12661567 2 Arthritis
126615672 12661567 3 Hypertension
126615672 12661567 4 Thyroid disorder
126615672 12661567 6 Eye disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126615672 12661567 Condition aggravated
126615672 12661567 Drug ineffective
126615672 12661567 Herpes zoster

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
126615672 12661567 1 20160621 0