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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103521362 | 10352136 | 2 | F | 20080526 | 20160325 | 20140730 | 20160726 | PER | US-ABBVIE-13P-163-1133884-00 | ABBVIE | 66.75 | YR | F | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103521362 | 10352136 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | Y | UNKNOWN | 21402 | 50 | UG | QD | ||||||
| 103521362 | 10352136 | 2 | SS | LEVOTHYROXINE SODIUM. | LEVOTHYROXINE SODIUM | 1 | Oral | U | 0 | ||||||||||
| 103521362 | 10352136 | 3 | SS | LEVOTHYROXINE SODIUM. | LEVOTHYROXINE SODIUM | 1 | Oral | U | 0 | ||||||||||
| 103521362 | 10352136 | 4 | SS | UNITHROID | LEVOTHYROXINE SODIUM | 1 | Oral | U | 0 | ||||||||||
| 103521362 | 10352136 | 5 | C | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
| 103521362 | 10352136 | 6 | C | VITAMINS | VITAMINS | 1 | 0 | ||||||||||||
| 103521362 | 10352136 | 7 | C | ARMOUR THYROID | THYROID, PORCINE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 103521362 | 10352136 | 1 | Hypothyroidism |
| 103521362 | 10352136 | 2 | Hypothyroidism |
| 103521362 | 10352136 | 3 | Hypothyroidism |
| 103521362 | 10352136 | 4 | Hypothyroidism |
| 103521362 | 10352136 | 5 | Hypothyroidism |
| 103521362 | 10352136 | 6 | Product used for unknown indication |
| 103521362 | 10352136 | 7 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 103521362 | 10352136 | Drug hypersensitivity | |
| 103521362 | 10352136 | Dyspnoea exertional |
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 |
|---|---|---|---|---|---|---|
| 103521362 | 10352136 | 1 | 20080519 | 20090308 | 0 | |
| 103521362 | 10352136 | 5 | 20090425 | 0 | ||
| 103521362 | 10352136 | 7 | 2009 | 20090425 | 0 |