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
123908612 12390861 2 F 20150212 20160720 20160520 20160726 EXP BR-ABBVIE-16P-020-1633983-00 ABBVIE 63.86 YR F Y 70.00000 KG 20160726 CN COUNTRY NOT SPECIFIED BR

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
123908612 12390861 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral IN FASTING UNKNOWN 21402
123908612 12390861 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown UNKNOWN 21402
123908612 12390861 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown UNKNOWN 21402
123908612 12390861 4 C ALDACTONE SPIRONOLACTONE 1 Oral 0
123908612 12390861 5 C AMIODARONE AMIODARONE 1 Oral DAILY DOSE: 200 MG; 1 TABLET ONCE A DAY, AT NIGHT 0 200 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123908612 12390861 1 Hypothyroidism
123908612 12390861 4 Arrhythmia
123908612 12390861 5 Arrhythmia

Outcome of event

Event ID CASEID OUTC COD
123908612 12390861 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
123908612 12390861 Myocardial infarction
123908612 12390861 Weight decreased

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
123908612 12390861 1 2006 0