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
125929791 12592979 1 I 201506 20150824 20160726 20160726 PER US-ABBVIE-15P-163-1451185-00 ABBVIE 91.07 YR F Y 54.48000 KG 20160726 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
125929791 12592979 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 1031969 21402 TABLET
125929791 12592979 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 TABLET
125929791 12592979 3 C PROLIA DENOSUMAB 1 0
125929791 12592979 4 C ELIQUIS APIXABAN 1 0
125929791 12592979 5 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125929791 12592979 1 Hypothyroidism
125929791 12592979 2 Hypothyroidism
125929791 12592979 3 Bone disorder
125929791 12592979 4 Atrial fibrillation
125929791 12592979 5 Atrial fibrillation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125929791 12592979 Adverse drug reaction
125929791 12592979 Blood thyroid stimulating hormone abnormal
125929791 12592979 Rash generalised

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
125929791 12592979 1 201506 0
125929791 12592979 2 201506 0