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
126915631 12691563 1 I 20160728 20160825 20160826 20160826 EXP CO-ABBVIE-16P-036-1712076-00 ABBVIE 68.00 YR M Y 67.10000 KG 20160826 OT COUNTRY NOT SPECIFIED CO

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
126915631 12691563 1 PS ZEMPLAR PARICALCITOL 1 Oral UNKNOWN 20819 1 UG CAPSULE QD
126915631 12691563 2 C CLONIDINE. CLONIDINE 1 0
126915631 12691563 3 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 0
126915631 12691563 4 C ACETYLSALICYLIC ACID ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126915631 12691563 1 Hyperparathyroidism secondary
126915631 12691563 2 Product used for unknown indication
126915631 12691563 3 Product used for unknown indication
126915631 12691563 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126915631 12691563 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126915631 12691563 Cerebrovascular accident
126915631 12691563 Disorientation
126915631 12691563 General physical health deterioration
126915631 12691563 Headache

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
126915631 12691563 1 20151124 20160727 0