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
126710922 12671092 2 F 20160831 20160822 20160905 EXP CA-ROCHE-1817135 ROCHE 0.00 F Y 0.00000 20160905 MD CA CA

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
126710922 12671092 1 PS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown 1000 MG/D U 50722
126710922 12671092 2 C COVERSYL PERINDOPRIL 1 0
126710922 12671092 3 C COUMADIN WARFARIN SODIUM 1 0
126710922 12671092 4 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126710922 12671092 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126710922 12671092 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126710922 12671092 Amnesia
126710922 12671092 Antiphospholipid syndrome
126710922 12671092 Autoimmune hepatitis
126710922 12671092 Cerebrovascular accident
126710922 12671092 Diarrhoea
126710922 12671092 Drug ineffective
126710922 12671092 Hypertension
126710922 12671092 Nephritis
126710922 12671092 Obstructive airways disorder
126710922 12671092 Osteoarthritis
126710922 12671092 Systemic lupus erythematosus

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
126710922 12671092 1 200711 0