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
126564471 12656447 1 I 201602 20160809 20160816 20160816 EXP US-ABBVIE-16P-163-1698510-00 ABBVIE 73.88 YR M Y 0.00000 20160816 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
126564471 12656447 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Unknown DOSE DECREASED UNKNOWN 18723
126564471 12656447 2 SS DEPAKOTE DIVALPROEX SODIUM 1 Unknown UNKNOWN 18723
126564471 12656447 3 SS AZILECT RASAGILINE MESYLATE 1 Unknown DOSE DECREASED UNKNOWN 0
126564471 12656447 4 SS AZILECT RASAGILINE MESYLATE 1 Unknown UNKNOWN 0
126564471 12656447 5 C CELEXA CITALOPRAM HYDROBROMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126564471 12656447 1 Product used for unknown indication
126564471 12656447 3 Parkinson's disease
126564471 12656447 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126564471 12656447 OT
126564471 12656447 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126564471 12656447 Arthropathy
126564471 12656447 Chills
126564471 12656447 Fall
126564471 12656447 Femur fracture
126564471 12656447 Hyperhidrosis
126564471 12656447 Muscular weakness
126564471 12656447 Nasopharyngitis

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
126564471 12656447 1 201602 0
126564471 12656447 3 2009 201602 0
126564471 12656447 4 201602 0