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
126531581 12653158 1 I 201606 20160726 20160815 20160815 EXP AR-ABBVIE-16P-007-1692948-00 ABBVIE 59.79 YR F Y 0.00000 20160815 CN COUNTRY NOT SPECIFIED AR

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
126531581 12653158 1 PS ZEMPLAR PARICALCITOL 1 Oral UNKNOWN 21606 2 UG CAPSULE QD
126531581 12653158 2 C ATENOLOL. ATENOLOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126531581 12653158 1 Hyperparathyroidism secondary
126531581 12653158 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126531581 12653158 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126531581 12653158 Anaemia
126531581 12653158 Bronchitis
126531581 12653158 Drug ineffective
126531581 12653158 Dyspnoea
126531581 12653158 Fall
126531581 12653158 Hypertension
126531581 12653158 Pain
126531581 12653158 Productive cough

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
126531581 12653158 1 20140728 0