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
123760833 12376083 3 F 20160830 20160517 20160831 EXP CA-BEH-2016062596 CSL BEHRING 53.00 YR A F Y 0.00000 20160831 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
123760833 12376083 1 PS HIZENTRA HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 4G VIALS 4358400026 125350 INJECTION
123760833 12376083 2 SS HIZENTRA HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 1G VIALS 4358100018 125350 INJECTION
123760833 12376083 3 SS HIZENTRA HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 25 CC (CUBIC CENTIMETRES). ONGOING. PUMP. 125350 INJECTION BIW
123760833 12376083 4 SS IVIG HUMAN IMMUNOGLOBULIN G 1 0
123760833 12376083 5 SS TOPAMAX TOPIRAMATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123760833 12376083 1 Primary immunodeficiency syndrome
123760833 12376083 2 Immunodeficiency common variable
123760833 12376083 4 Product used for unknown indication
123760833 12376083 5 Headache

Outcome of event

Event ID CASEID OUTC COD
123760833 12376083 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123760833 12376083 Depression
123760833 12376083 Dizziness
123760833 12376083 Headache
123760833 12376083 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
123760833 12376083 3 201512 0