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
125935221 12593522 1 I 201509 20151218 20160726 20160726 PER US-ABBVIE-15P-163-1524139-00 ABBVIE 84.98 YR M Y 77.18000 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
125935221 12593522 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 TABLET
125935221 12593522 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 TABLET
125935221 12593522 3 C ASPIRIN. ASPIRIN 1 Unknown 0
125935221 12593522 4 C CLARITIN LORATADINE 1 Unknown 0
125935221 12593522 5 C HALCION TRIAZOLAM 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125935221 12593522 1 Hypothyroidism
125935221 12593522 2 Hypothyroidism
125935221 12593522 3 Product used for unknown indication
125935221 12593522 4 Product used for unknown indication
125935221 12593522 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125935221 12593522 Diarrhoea
125935221 12593522 Flatulence
125935221 12593522 Frequent bowel movements
125935221 12593522 Myalgia

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
125935221 12593522 1 201509 201509 0
125935221 12593522 2 201509 201509 0