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
124696222 12469622 2 F 201605 20160725 20160615 20160729 EXP GB-ABBVIE-16P-167-1653555-00 ABBVIE 58.00 YR F Y 0.00000 20160729 MD GB GB

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
124696222 12469622 1 PS VALPROATE SODIUM. VALPROATE SODIUM 1 Unknown Y UNKNOWN 18081
124696222 12469622 2 SS ZAPONEX CLOZAPINE 1 Oral UNKNOWN 0 TABLET
124696222 12469622 3 SS ZAPONEX CLOZAPINE 1 Oral UNKNOWN 0 TABLET
124696222 12469622 4 SS ZAPONEX CLOZAPINE 1 Oral UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124696222 12469622 1 Product used for unknown indication
124696222 12469622 2 Schizophrenia

Outcome of event

Event ID CASEID OUTC COD
124696222 12469622 LT
124696222 12469622 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124696222 12469622 Agranulocytosis
124696222 12469622 Drug monitoring procedure incorrectly performed
124696222 12469622 Leukopenia
124696222 12469622 Nausea
124696222 12469622 Neutropenia
124696222 12469622 Neutrophil count decreased
124696222 12469622 Vomiting

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
124696222 12469622 1 201605 0
124696222 12469622 2 20140829 20150808 0
124696222 12469622 3 20150813 201601 0
124696222 12469622 4 20160404 20160520 0