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
123753562 12375356 2 F 20160719 20160517 20160720 EXP CA-BEH-2016062707 CSL BEHRING 53.00 YR A F Y 0.00000 20160720 CN 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
123753562 12375356 1 PS IVIG HUMAN IMMUNOGLOBULIN G 1 Intravenous (not otherwise specified) 125201 INFUSION
123753562 12375356 2 SS HIZENTRA HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 4G VIALS 43584000261 0
123753562 12375356 3 SS HIZENTRA HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 4G VIALS 4358100018 0
123753562 12375356 4 SS HIZENTRA HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 25 CC (CUBIC CENTIMETRES). ONGOING. PUMP. 0 BIW
123753562 12375356 5 SS TOPAMAX TOPIRAMATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123753562 12375356 1 Product used for unknown indication
123753562 12375356 2 Primary immunodeficiency syndrome
123753562 12375356 3 Immunodeficiency common variable
123753562 12375356 5 Headache

Outcome of event

Event ID CASEID OUTC COD
123753562 12375356 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123753562 12375356 Depression
123753562 12375356 Dizziness
123753562 12375356 Headache
123753562 12375356 Vena cava thrombosis

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
123753562 12375356 4 201512 0