The Safety Rates Drug Report

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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
125616041 12561604 1 I 2011 20150605 20160715 20160715 PER US-IGSA-GTI003273 GRIFOLS 0.00 A F Y 0.00000 20160715 CN US US

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
125616041 12561604 1 PS GAMUNEX-C HUMAN IMMUNOGLOBULIN G 1 Intravenous (not otherwise specified) Y 125046 50 G INJECTION /month
125616041 12561604 2 SS HYDROCODONE HYDROCODONE 1 Y 0
125616041 12561604 3 SS FENTANYL. FENTANYL 1 Y 0
125616041 12561604 4 C ANTI-NAUSEA /00013304/ PROCHLORPERAZINE MALEATE 1 0
125616041 12561604 5 C FOLIC ACID. FOLIC ACID 1 0
125616041 12561604 6 C VITAMIN B12 CYANOCOBALAMIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125616041 12561604 1 Chronic inflammatory demyelinating polyradiculoneuropathy
125616041 12561604 4 Nausea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125616041 12561604 Fatigue Fatigue

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
125616041 12561604 1 2011 0