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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125475991 | 12547599 | 1 | I | 20160708 | 20160712 | 20160712 | EXP | US-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00295 | SCIEGEN | 34.00 | YR | M | Y | 0.00000 | 20160712 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125475991 | 12547599 | 1 | PS | Hydrochlorothiazide Tablets | HYDROCHLOROTHIAZIDE | 1 | Endocervical | UNK | U | U | 203018 | TABLET | |||||||
| 125475991 | 12547599 | 2 | SS | FEBUXOSTAT. | FEBUXOSTAT | 1 | Unknown | 40 MG DAILY | Y | U | 0 | 40 | MG | ||||||
| 125475991 | 12547599 | 3 | SS | COLCHICINE. | COLCHICINE | 1 | Unknown | 1.2 MG DAILY | U | U | 0 | 1.2 | MG | ||||||
| 125475991 | 12547599 | 4 | SS | ALLOPURINOL. | ALLOPURINOL | 1 | Unknown | 300 MG PER DAY | U | U | 0 | 300 | MG | ||||||
| 125475991 | 12547599 | 5 | SS | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125475991 | 12547599 | 6 | SS | LISINOPRIL. | LISINOPRIL | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125475991 | 12547599 | 7 | SS | RANITIDINE. | RANITIDINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125475991 | 12547599 | 8 | SS | Amitriptyline | AMITRIPTYLINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125475991 | 12547599 | 9 | SS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | 1-2 TABLETS PER DAY | U | U | 0 | ||||||||
| 125475991 | 12547599 | 10 | SS | Codeine | CODEINE | 1 | Unknown | 1-2 TABLETS PER DAY | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125475991 | 12547599 | 1 | Product used for unknown indication |
| 125475991 | 12547599 | 2 | Product used for unknown indication |
| 125475991 | 12547599 | 3 | Product used for unknown indication |
| 125475991 | 12547599 | 4 | Product used for unknown indication |
| 125475991 | 12547599 | 5 | Product used for unknown indication |
| 125475991 | 12547599 | 6 | Product used for unknown indication |
| 125475991 | 12547599 | 7 | Product used for unknown indication |
| 125475991 | 12547599 | 8 | Product used for unknown indication |
| 125475991 | 12547599 | 9 | Product used for unknown indication |
| 125475991 | 12547599 | 10 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125475991 | 12547599 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125475991 | 12547599 | Abdominal pain | |
| 125475991 | 12547599 | Blood bilirubin increased | |
| 125475991 | 12547599 | Cholelithiasis | |
| 125475991 | 12547599 | Cholestasis | |
| 125475991 | 12547599 | Chromaturia | |
| 125475991 | 12547599 | Fatigue | |
| 125475991 | 12547599 | Hepatic necrosis | |
| 125475991 | 12547599 | Jaundice | |
| 125475991 | 12547599 | Nausea | |
| 125475991 | 12547599 | Necrosis | |
| 125475991 | 12547599 | Obesity | |
| 125475991 | 12547599 | Pancreatitis acute | |
| 125475991 | 12547599 | Pruritus |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |