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
125928971 12592897 1 I 201511 20151120 20160726 20160726 PER US-ABBVIE-15P-163-1512151-00 ABBVIE 52.94 YR F Y 83.99000 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
125928971 12592897 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral TAKES AT 6 AM DAILY UNKNOWN 21402 50 UG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125928971 12592897 1 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125928971 12592897 Chest discomfort
125928971 12592897 Dizziness
125928971 12592897 Feeling abnormal
125928971 12592897 Lip swelling

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
125928971 12592897 1 201511 0