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
125223893 12522389 3 F 2016 20160718 20160701 20160726 EXP CA-ABBVIE-16P-028-1666294-00 ABBVIE 0.00 M Y 0.00000 20160726 CN CA CA

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
125223893 12522389 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown N UNKNOWN 21402
125223893 12522389 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 150MCG N UNKNOWN 21402
125223893 12522389 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 137MCG N UNKNOWN 21402

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125223893 12522389 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125223893 12522389 HO
125223893 12522389 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125223893 12522389 Diabetes mellitus
125223893 12522389 Dysphagia
125223893 12522389 Dyspnoea
125223893 12522389 Fatigue
125223893 12522389 Headache
125223893 12522389 Hyperhidrosis
125223893 12522389 Hyperthyroidism
125223893 12522389 Incorrect dose administered
125223893 12522389 Parkinson's disease
125223893 12522389 Pruritus
125223893 12522389 Pyrexia
125223893 12522389 Tongue spasm
125223893 12522389 Tremor
125223893 12522389 Weight decreased

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

no results found

Therapies reported

no results found