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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122167242 | 12216724 | 2 | F | 20160912 | 20160329 | 20160927 | EXP | US-AUROBINDO-AUR-APL-2016-03819 | AUROBINDO | 82.00 | YR | M | Y | 50.00000 | KG | 20160927 | OT | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122167242 | 12216724 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Unknown | 500 MG, TWO TIMES A DAY | U | 77859 | 500 | MG | BID | ||||||
| 122167242 | 12216724 | 2 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 20 MG, EVERY MORNING | U | U | 0 | 20 | MG | ||||||
| 122167242 | 12216724 | 3 | C | SOLIFENACIN SUCCINATE. | SOLIFENACIN SUCCINATE | 1 | Oral | 5 MG, EVERY MORNING | U | U | 0 | 5 | MG | ||||||
| 122167242 | 12216724 | 4 | C | SOLIFENACIN SUCCINATE. | SOLIFENACIN SUCCINATE | 1 | Oral | EVERY MORNING | U | U | 0 | 5 | MG | ||||||
| 122167242 | 12216724 | 5 | C | ALENDRONATE | ALENDRONATE SODIUM | 1 | Oral | 70 MG, EVERY WEEK | U | 0 | 70 | MG | /wk | ||||||
| 122167242 | 12216724 | 6 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Oral | 325 MG, TWO TIMES A DAY | U | 0 | 325 | MG | BID | ||||||
| 122167242 | 12216724 | 7 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Oral | U | 0 | 325 | MG | BID | |||||||
| 122167242 | 12216724 | 8 | C | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 37.5 MG, EVERY MORNING | U | 0 | 37.5 | MG | |||||||
| 122167242 | 12216724 | 9 | C | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | EVERY MORNING | U | 0 | 37.5 | MG | |||||||
| 122167242 | 12216724 | 10 | C | ASPIRIN. | ASPIRIN | 1 | Oral | 81 MG, DAILY | U | 0 | 81 | MG | ENTERIC COATED TABLET | ||||||
| 122167242 | 12216724 | 11 | C | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Unknown | 25 MG, TWO TIMES A DAY | U | 0 | 25 | MG | BID | ||||||
| 122167242 | 12216724 | 12 | C | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | U | 0 | 25 | MG | BID | |||||||
| 122167242 | 12216724 | 13 | C | CALCIUM CARBONATE. | CALCIUM CARBONATE | 1 | Oral | 600 MG, TWO TIMES A DAY | U | 0 | 600 | MG | BID | ||||||
| 122167242 | 12216724 | 14 | C | CALCIUM CARBONATE. | CALCIUM CARBONATE | 1 | Oral | U | 0 | 600 | MG | BID | |||||||
| 122167242 | 12216724 | 15 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | 650 MG, EVERY EIGHT HOURS | U | 0 | 650 | MG | |||||||
| 122167242 | 12216724 | 16 | C | BETAMETHASONE VALERATE W/CLOTRIMAZOLE | 2 | Topical | UNK, TWO TIMES A DAY | U | 0 | CREAM | BID | ||||||||
| 122167242 | 12216724 | 17 | C | B-LABOTEROL | 2 | Topical | U | 0 | |||||||||||
| 122167242 | 12216724 | 18 | C | LOPERAMIDE HYDROCHLORIDE. | LOPERAMIDE HYDROCHLORIDE | 1 | Oral | 2 MG, UNK | U | 0 | 2 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122167242 | 12216724 | 1 | Urinary tract infection |
| 122167242 | 12216724 | 2 | Product used for unknown indication |
| 122167242 | 12216724 | 3 | Product used for unknown indication |
| 122167242 | 12216724 | 5 | Product used for unknown indication |
| 122167242 | 12216724 | 6 | Product used for unknown indication |
| 122167242 | 12216724 | 8 | Product used for unknown indication |
| 122167242 | 12216724 | 10 | Product used for unknown indication |
| 122167242 | 12216724 | 11 | Product used for unknown indication |
| 122167242 | 12216724 | 13 | Product used for unknown indication |
| 122167242 | 12216724 | 15 | Product used for unknown indication |
| 122167242 | 12216724 | 16 | Product used for unknown indication |
| 122167242 | 12216724 | 17 | Product used for unknown indication |
| 122167242 | 12216724 | 18 | Diarrhoea |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122167242 | 12216724 | HO |
| 122167242 | 12216724 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122167242 | 12216724 | Asthenia | |
| 122167242 | 12216724 | Dehydration | |
| 122167242 | 12216724 | Diarrhoea | |
| 122167242 | 12216724 | Enterocolitis bacterial | |
| 122167242 | 12216724 | Faeces discoloured | |
| 122167242 | 12216724 | Gastrointestinal haemorrhage | |
| 122167242 | 12216724 | Leukocytosis | |
| 122167242 | 12216724 | Nausea | |
| 122167242 | 12216724 | Pneumonia aspiration | |
| 122167242 | 12216724 | Sepsis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |