The Safety Rates Drug Report

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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
125930911 12593091 1 I 201508 20151130 20160726 20160726 PER US-ABBVIE-15P-163-1515362-00 ABBVIE 88.00 YR M Y 60.00000 KG 20160726 MD 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
125930911 12593091 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral HALF TABLET UNKNOWN 21402 25 UG TABLET QD
125930911 12593091 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral HALF TABLET UNKNOWN 21402 12.5 UG TABLET QD
125930911 12593091 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral N UNKNOWN,UNKNOWN 21402 50 UG TABLET QD
125930911 12593091 4 C PEPCID FAMOTIDINE 1 Unknown 0
125930911 12593091 5 C XANAX ALPRAZOLAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125930911 12593091 1 Hypothyroidism
125930911 12593091 3 Hypothyroidism
125930911 12593091 4 Gastrooesophageal reflux disease
125930911 12593091 5 Neuropathy peripheral

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125930911 12593091 Balance disorder
125930911 12593091 Headache
125930911 12593091 Nausea
125930911 12593091 Vertigo

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
125930911 12593091 1 2015 0
125930911 12593091 2 2015 0
125930911 12593091 3 201508 0