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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126766901 | 12676690 | 1 | I | 20160809 | 20160823 | 20160823 | EXP | KR-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-122674 | RANBAXY | 45.00 | YR | M | Y | 0.00000 | 20160823 | OT | GB | KR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126766901 | 12676690 | 1 | PS | Esomeprazole | ESOMEPRAZOLE | 1 | Intravenous (not otherwise specified) | UNK | Y | 200882 | |||||||||
| 126766901 | 12676690 | 2 | C | LACTULOSE. | LACTULOSE | 1 | Oral | UNK | U | 0 | |||||||||
| 126766901 | 12676690 | 3 | C | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Unknown | 160/4.5?G | U | 0 | INHALATION POWDER | ||||||||
| 126766901 | 12676690 | 4 | C | Candesartan | CANDESARTAN | 1 | Unknown | 8 MG, DAILY | U | 0 | 8 | MG | |||||||
| 126766901 | 12676690 | 5 | C | Acetyl salicylic acid | ASPIRIN | 1 | Unknown | 100 MG, DAILY | U | 0 | 100 | MG | |||||||
| 126766901 | 12676690 | 6 | C | Atorvastatin | ATORVASTATIN | 1 | Unknown | 10 MG, DAILY | U | 0 | 10 | MG | |||||||
| 126766901 | 12676690 | 7 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Unknown | 75 MG, DAILY | U | 0 | 75 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126766901 | 12676690 | 1 | Gastrooesophageal reflux disease |
| 126766901 | 12676690 | 2 | Constipation |
| 126766901 | 12676690 | 3 | Asthma |
| 126766901 | 12676690 | 4 | Product used for unknown indication |
| 126766901 | 12676690 | 5 | Product used for unknown indication |
| 126766901 | 12676690 | 6 | Product used for unknown indication |
| 126766901 | 12676690 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126766901 | 12676690 | OT |
| 126766901 | 12676690 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126766901 | 12676690 | Rhabdomyolysis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |