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
125337771 12533777 1 I 201602 20160627 20160706 20160706 EXP US-TEVA-672692USA TEVA 0.00 M Y 0.00000 20160707 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
125337771 12533777 1 PS AZILECT RASAGILINE MESYLATE 1 1 MILLIGRAM DAILY; Y 21641 1 MG QD
125337771 12533777 2 SS DEPAKOTE DIVALPROEX SODIUM 1 Y 0
125337771 12533777 3 C CELEXA CITALOPRAM HYDROBROMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125337771 12533777 1 Parkinson's disease

Outcome of event

Event ID CASEID OUTC COD
125337771 12533777 HO
125337771 12533777 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125337771 12533777 Abasia
125337771 12533777 Asthenia
125337771 12533777 Chills
125337771 12533777 Condition aggravated
125337771 12533777 Fall
125337771 12533777 Hyperhidrosis
125337771 12533777 Lower limb fracture
125337771 12533777 Tremor

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
125337771 12533777 1 2009 0
125337771 12533777 2 201509 0