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
125931161 12593116 1 I 2015 20160331 20160726 20160726 PER US-ABBVIE-16P-163-1596204-00 ABBVIE 0.00 F Y 0.00000 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
125931161 12593116 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 TABLET
125931161 12593116 2 SS PREMARIN ESTROGENS, CONJUGATED 1 Oral UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125931161 12593116 1 Hypothyroidism
125931161 12593116 2 Oestrogen replacement therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125931161 12593116 Blood glucose increased
125931161 12593116 Blood thyroid stimulating hormone decreased
125931161 12593116 Fatigue
125931161 12593116 Food craving

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found