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
126376261 12637626 1 I 199409 19940919 20160809 20160809 PER US-ABBVIE-94P-163-0040244-00 ABBVIE 25.00 YR M Y 74.91000 KG 20160809 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
126376261 12637626 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Oral Y UNKNOWN 18723 2 G
126376261 12637626 2 SS DEPAKOTE DIVALPROEX SODIUM 1 Y UNKNOWN 18723
126376261 12637626 3 SS DEPAKOTE DIVALPROEX SODIUM 1 Y UNKNOWN 18723
126376261 12637626 4 SS DEPAKOTE DIVALPROEX SODIUM 1 Y UNKNOWN 18723
126376261 12637626 5 SS DEPAKOTE DIVALPROEX SODIUM 1 Y UNKNOWN 18723

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126376261 12637626 1 Cluster headache

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126376261 12637626 Anxiety
126376261 12637626 Drug level increased
126376261 12637626 Frustration tolerance decreased
126376261 12637626 Incorrect dose administered
126376261 12637626 Malaise
126376261 12637626 Off label use
126376261 12637626 Pain
126376261 12637626 Stress
126376261 12637626 Toxicity to various agents

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
126376261 12637626 1 199403 0