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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126895381 | 12689538 | 1 | I | 20160616 | 20160815 | 20160826 | 20160826 | EXP | DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-122790 | RANBAXY | 34.00 | YR | F | Y | 70.00000 | KG | 20160826 | OT | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126895381 | 12689538 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | Oral | UNK | U | 0 | |||||||||
| 126895381 | 12689538 | 2 | C | L-Thyroxine | LEVOTHYROXINE | 1 | Oral | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126895381 | 12689538 | 1 | Sinusitis |
| 126895381 | 12689538 | 2 | Hypothyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126895381 | 12689538 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126895381 | 12689538 | Hepatitis acute | |
| 126895381 | 12689538 | Rash generalised |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |