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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127050131 | 12705013 | 1 | I | 20160828 | 0 | 20160831 | 20160831 | DIR | 62.00 | YR | F | N | 165.00000 | LBS | 20160829 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127050131 | 12705013 | 1 | PS | AZITHROMYCIN ANHYDROUS. | AZITHROMYCIN ANHYDROUS | 1 | Oral | N | D | GF7491 | 20180228 | 0 | 2 | DF | COATED TABLET | QD | |||
| 127050131 | 12705013 | 3 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
| 127050131 | 12705013 | 4 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127050131 | 12705013 | 1 | Sinusitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127050131 | 12705013 | RI |
| 127050131 | 12705013 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127050131 | 12705013 | Dizziness | |
| 127050131 | 12705013 | Eyelid ptosis | |
| 127050131 | 12705013 | Impaired driving ability | |
| 127050131 | 12705013 | Palpitations | |
| 127050131 | 12705013 | Vision blurred |
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 |
|---|---|---|---|---|---|---|
| 127050131 | 12705013 | 1 | 20160826 | 20160828 | 0 |