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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119130042 | 11913004 | 2 | F | 20160830 | 20160113 | 20160913 | EXP | GB-AUROBINDO-AUR-APL-2016-00053 | AUROBINDO | 31.00 | YR | F | Y | 0.00000 | 20160913 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119130042 | 11913004 | 1 | PS | DIDANOSINE. | DIDANOSINE | 1 | Unknown | UNK | U | U | 77275 | ||||||||
| 119130042 | 11913004 | 2 | SS | DIDANOSINE. | DIDANOSINE | 1 | Unknown | UNK | U | U | 77275 | ||||||||
| 119130042 | 11913004 | 3 | SS | STAVUDINE. | STAVUDINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 119130042 | 11913004 | 4 | SS | STAVUDINE. | STAVUDINE | 1 | U | U | 0 | ||||||||||
| 119130042 | 11913004 | 5 | SS | VIRAMUNE | NEVIRAPINE | 1 | Unknown | 200 MG, UNK | U | U | 0 | 200 | MG | ||||||
| 119130042 | 11913004 | 6 | SS | VIRAMUNE | NEVIRAPINE | 1 | Unknown | 200 MG, UNK | U | U | 0 | 200 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119130042 | 11913004 | 1 | Product used for unknown indication |
| 119130042 | 11913004 | 2 | Product used for unknown indication |
| 119130042 | 11913004 | 3 | Product used for unknown indication |
| 119130042 | 11913004 | 4 | Product used for unknown indication |
| 119130042 | 11913004 | 5 | Product used for unknown indication |
| 119130042 | 11913004 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119130042 | 11913004 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119130042 | 11913004 | Exposure during pregnancy | |
| 119130042 | 11913004 | Hepatic steatosis | |
| 119130042 | 11913004 | Lactic acidosis | |
| 119130042 | 11913004 | Live birth | |
| 119130042 | 11913004 | Pancreatitis | |
| 119130042 | 11913004 | Pregnancy |
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 |
|---|---|---|---|---|---|---|
| 119130042 | 11913004 | 3 | 2001 | 0 |