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
125930331 12593033 1 I 20160324 20160726 20160726 PER US-ABBVIE-16P-163-1593456-00 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
125930331 12593033 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 100 UG TABLET QD
125930331 12593033 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 88 UG TABLET QD
125930331 12593033 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 75 UG TABLET QD
125930331 12593033 4 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 75 UG TABLET QD
125930331 12593033 5 C KEPPRA LEVETIRACETAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125930331 12593033 1 Hypothyroidism
125930331 12593033 5 Seizure

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125930331 12593033 Heart rate increased
125930331 12593033 Palpitations
125930331 12593033 Tremor
125930331 12593033 Weight decreased

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
125930331 12593033 1 2015 2015 0
125930331 12593033 2 2015 2015 0
125930331 12593033 3 2016 2016 0
125930331 12593033 4 2016 0