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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126402642 | 12640264 | 2 | F | 20160729 | 20160810 | 20160810 | EXP | GB-ACTAVISPR-2016-17129 | ACTAVIS | 46.00 | YR | F | Y | 0.00000 | 20160810 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126402642 | 12640264 | 1 | SS | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Oral | 40 MG, UNK | U | UNCONFIRMED | 0 | 40 | MG | UNK | |||||
| 126402642 | 12640264 | 2 | PS | Spironolactone (Unknown) | SPIRONOLACTONE | 1 | Oral | 100 MG, UNK | U | UNCONFIRMED | 40353 | 100 | MG | UNK | |||||
| 126402642 | 12640264 | 3 | SS | Tenofovir (Unknown) | TENOFOVIR | 1 | Oral | 245 MG, UNK | U | UNCONFIRMED | 0 | 245 | MG | UNK | |||||
| 126402642 | 12640264 | 4 | SS | BACTRIM | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Oral | UNK (80/400MG) | U | 0 | |||||||||
| 126402642 | 12640264 | 5 | SS | DARUNAVIR | DARUNAVIR | 1 | Oral | 800 MG, UNK | U | 0 | 800 | MG | |||||||
| 126402642 | 12640264 | 6 | SS | EMTRICITABINE | EMTRICITABINE | 1 | Oral | 200 MG, UNK | U | 0 | 200 | MG | |||||||
| 126402642 | 12640264 | 7 | SS | NORVIR | RITONAVIR | 1 | Oral | 100 MG, UNK | U | 0 | 100 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126402642 | 12640264 | 1 | Product used for unknown indication |
| 126402642 | 12640264 | 2 | Product used for unknown indication |
| 126402642 | 12640264 | 3 | Product used for unknown indication |
| 126402642 | 12640264 | 4 | Product used for unknown indication |
| 126402642 | 12640264 | 5 | Product used for unknown indication |
| 126402642 | 12640264 | 6 | Product used for unknown indication |
| 126402642 | 12640264 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126402642 | 12640264 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126402642 | 12640264 | Cerebrovascular accident |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |