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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127173321 | 12717332 | 1 | I | 201607 | 20160829 | 20160906 | 20160906 | EXP | US-PFIZER INC-2016409965 | PFIZER | 8.00 | YR | M | Y | 0.00000 | 20160906 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127173321 | 12717332 | 1 | PS | FLAGYL | METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE | 1 | UNK | U | 12623 | ||||||||||
| 127173321 | 12717332 | 2 | SS | AMBRISENTAN | AMBRISENTAN | 1 | Oral | 5 MG, DAILY | 1412805A | 0 | 5 | MG | TABLET | ||||||
| 127173321 | 12717332 | 3 | C | BABY ASPIRIN | ASPIRIN | 1 | UNK | 0 | |||||||||||
| 127173321 | 12717332 | 4 | C | ADCIRCA | TADALAFIL | 1 | UNK | 0 | |||||||||||
| 127173321 | 12717332 | 5 | C | TYVASO | TREPROSTINIL | 1 | UNK | 0 | |||||||||||
| 127173321 | 12717332 | 6 | C | PYRIDOXINE | PYRIDOXINE | 1 | UNK | 0 | |||||||||||
| 127173321 | 12717332 | 7 | C | LEVETIRACETAM. | LEVETIRACETAM | 1 | UNK | 0 | |||||||||||
| 127173321 | 12717332 | 8 | C | FUROSEMIDE. | FUROSEMIDE | 1 | UNK | 0 | |||||||||||
| 127173321 | 12717332 | 9 | C | DIASTAT ACUDIAL | DIAZEPAM | 1 | UNK | 0 | |||||||||||
| 127173321 | 12717332 | 10 | C | TUMS KIDS | 2 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127173321 | 12717332 | 2 | Pulmonary arterial hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127173321 | 12717332 | HO |
| 127173321 | 12717332 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127173321 | 12717332 | Adenotonsillectomy | |
| 127173321 | 12717332 | Arthralgia | |
| 127173321 | 12717332 | Arthritis reactive | |
| 127173321 | 12717332 | Clostridium difficile infection | |
| 127173321 | 12717332 | Joint swelling | |
| 127173321 | 12717332 | Product use issue | |
| 127173321 | 12717332 | Weight bearing difficulty |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |