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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125931921 | 12593192 | 1 | I | 20160502 | 20160726 | 20160726 | PER | US-ABBVIE-16P-163-1619650-00 | ABBVIE | 0.00 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125931921 | 12593192 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | U | UNKNOWN | 21402 | |||||||||
125931921 | 12593192 | 2 | SS | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Oral | U | 0 | ||||||||||
125931921 | 12593192 | 3 | SS | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | Oral | U | 0 | 125 | UG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125931921 | 12593192 | 1 | Product used for unknown indication |
125931921 | 12593192 | 2 | Product used for unknown indication |
125931921 | 12593192 | 3 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125931921 | 12593192 | Asthenia | |
125931921 | 12593192 | Sinus headache | |
125931921 | 12593192 | Upper-airway cough syndrome |
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 |
---|---|---|---|---|---|---|
125931921 | 12593192 | 1 | 1980 | 0 |