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
105880204 10588020 4 F 20160705 20141117 20160708 EXP US-PFIZER INC-2014299718 PFIZER 68.00 YR F Y 54.00000 KG 20160708 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
105880204 10588020 1 PS LEVOXYL LEVOTHYROXINE SODIUM 1 UNK U 21301 TABLET
105880204 10588020 2 SS LEVOXYL LEVOTHYROXINE SODIUM 1 1 DF (0.05 TABLET), ONCE A DAY U 21301 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105880204 10588020 1 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
105880204 10588020 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105880204 10588020 Activities of daily living impaired
105880204 10588020 Anaphylactic reaction
105880204 10588020 Angina pectoris
105880204 10588020 Blood pressure decreased
105880204 10588020 Blood pressure diastolic decreased
105880204 10588020 Diarrhoea
105880204 10588020 Feeling abnormal
105880204 10588020 Palpitations
105880204 10588020 Product quality issue
105880204 10588020 Shock
105880204 10588020 Syncope

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
105880204 10588020 1 2013 0
105880204 10588020 2 201408 0