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
126477722 12647772 2 F 20160728 20160809 20160812 20160816 EXP IT-PFIZER INC-2016380692 PFIZER 28.00 YR Y 0.00000 20160816 MD IT IT

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
126477722 12647772 1 PS METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 1000 MG, DAILY 40664 1000 MG POWDER FOR INJECTION
126477722 12647772 2 SS ALEMTUZUMAB ALEMTUZUMAB 1 Intravenous (not otherwise specified) 12 MG, DAILY 0 12 MG
126477722 12647772 3 C ACICLOVIR ACYCLOVIR 1 Oral 400 MG, UNK 0 400 MG
126477722 12647772 4 C CETIRIZINE CETIRIZINE HYDROCHLORIDE 1 Oral 20 MG, UNK 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126477722 12647772 1 Premedication
126477722 12647772 2 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126477722 12647772 Pyrexia

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
126477722 12647772 1 20160627 20160701 0
126477722 12647772 2 20160627 20160701 0
126477722 12647772 3 20160626 20160801 0
126477722 12647772 4 20160626 20160702 0