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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126099691 | 12609969 | 1 | I | 20160709 | 20160719 | 20160801 | 20160801 | EXP | GB-AUROBINDO-AUR-APL-2016-09652 | AUROBINDO | 39.00 | YR | F | Y | 80.00000 | KG | 20160801 | MD | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126099691 | 12609969 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | U | 78021 | |||||||||
| 126099691 | 12609969 | 2 | C | ADALAT | NIFEDIPINE | 1 | Oral | 1 DF, ONCE A DAY | 224.957993 | DF | U | 0 | 1 | DF | QD | ||||
| 126099691 | 12609969 | 3 | C | BENDROFLUMETHIAZIDE | BENDROFLUMETHIAZIDE | 1 | Oral | 1 DF, ONCE A DAY, EACH MORNING. | 2 | DF | U | 0 | 1 | DF | QD | ||||
| 126099691 | 12609969 | 4 | C | LOSARTAN. | LOSARTAN | 1 | Oral | 1 DF, ONCE A DAY | 256.958008 | DF | U | 0 | 1 | DF | QD | ||||
| 126099691 | 12609969 | 5 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 2 DF, UNK | U | 0 | 2 | DF |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126099691 | 12609969 | 1 | Product used for unknown indication |
| 126099691 | 12609969 | 2 | Product used for unknown indication |
| 126099691 | 12609969 | 3 | Product used for unknown indication |
| 126099691 | 12609969 | 4 | Product used for unknown indication |
| 126099691 | 12609969 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126099691 | 12609969 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126099691 | 12609969 | Eye pain | |
| 126099691 | 12609969 | Headache | |
| 126099691 | 12609969 | Photophobia |
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 |
|---|---|---|---|---|---|---|
| 126099691 | 12609969 | 1 | 20160520 | 0 | ||
| 126099691 | 12609969 | 2 | 20151127 | 20160520 | 0 | |
| 126099691 | 12609969 | 3 | 20160711 | 0 | ||
| 126099691 | 12609969 | 4 | 20151026 | 0 | ||
| 126099691 | 12609969 | 5 | 20151026 | 0 |