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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126348201 | 12634820 | 1 | I | 20160722 | 0 | 20160808 | 20160808 | DIR | 61.00 | YR | F | N | 160.00000 | LBS | 20160805 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126348201 | 12634820 | 1 | PS | ALLEGRA ALLERGY | FEXOFENADINE HYDROCHLORIDE | 1 | Oral | ALLEGRA ALLERGY 180 MG?1 TABLET ONCE A DAY?TAKEN BY MOUTH | Y | D | HC104C | 20180731 | 0 | 1 | DF | COATED TABLET | QD | ||
| 126348201 | 12634820 | 3 | C | LEVOTHYROXIN | LEVOTHYROXINE | 1 | 0 | ||||||||||||
| 126348201 | 12634820 | 5 | C | ATENELOL | ATENOLOL | 1 | 0 | ||||||||||||
| 126348201 | 12634820 | 7 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | 0 | ||||||||||||
| 126348201 | 12634820 | 9 | C | HYDROCHOLOQUINE | 2 | 0 | |||||||||||||
| 126348201 | 12634820 | 11 | C | LOVOZA | 2 | 0 | |||||||||||||
| 126348201 | 12634820 | 13 | C | LIALDA | MESALAMINE | 1 | 0 | ||||||||||||
| 126348201 | 12634820 | 15 | C | TRIAM/HCTZ | 2 | 0 | |||||||||||||
| 126348201 | 12634820 | 17 | C | HUMIRA IBJECTIONS | 2 | 0 | |||||||||||||
| 126348201 | 12634820 | 19 | C | CENTRUM SENIOR | 2 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126348201 | 12634820 | 1 | Hypersensitivity |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126348201 | 12634820 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126348201 | 12634820 | Eye irritation | |
| 126348201 | 12634820 | Ocular discomfort | |
| 126348201 | 12634820 | Ocular hyperaemia | |
| 126348201 | 12634820 | 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 |
|---|---|---|---|---|---|---|
| 126348201 | 12634820 | 1 | 20160710 | 20160801 | 0 |