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
124539213 12453921 3 F 20160919 20160609 20160921 EXP AU-BEH-2016070096 CSL BEHRING 0.00 F Y 0.00000 20160921 CN AU AU

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
124539213 12453921 1 PS Human Immunoglobulin IV BMW (INN) HUMAN IMMUNOGLOBULIN G 1 Intravenous (not otherwise specified) UNK, QMT 125201 /month
124539213 12453921 2 SS METHOBLASTIN /00113801/ METHOTREXATE 1 Unknown 20 MG, QW 0 20 MG TABLET /wk
124539213 12453921 3 SS PREDNISOLONE. PREDNISOLONE 1 Unknown 25 MG, UNK 0 25 MG
124539213 12453921 4 SS FOLIC ACID. FOLIC ACID 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124539213 12453921 1 Dermatomyositis
124539213 12453921 2 Dermatomyositis
124539213 12453921 3 Dermatomyositis
124539213 12453921 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124539213 12453921 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124539213 12453921 Alopecia
124539213 12453921 Eye haemorrhage
124539213 12453921 Eye oedema
124539213 12453921 Haematoma
124539213 12453921 Inflammation

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found