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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127802262 | 12780226 | 2 | F | 201603 | 20160922 | 20160926 | 20160929 | EXP | US-PFIZER INC-2016444919 | PFIZER | 65.00 | YR | M | Y | 78.00000 | KG | 20160929 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127802262 | 12780226 | 1 | PS | SIROLIMUS. | SIROLIMUS | 1 | 2 MG, 2X/DAY(IN THE MORING AND AT NIGHT) | D | 21083 | 2 | MG | ORAL SOLUTION | BID | ||||||
127802262 | 12780226 | 2 | SS | SIROLIMUS. | SIROLIMUS | 1 | 2 MG, 1X/DAY(IN THE MORNING) | D | 21083 | 2 | MG | ORAL SOLUTION | QD | ||||||
127802262 | 12780226 | 3 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 20 MG, 1X/DAY | 0 | 20 | MG | QD | ||||||||
127802262 | 12780226 | 4 | C | ALLOPURINOL. | ALLOPURINOL | 1 | 150 MG, 1X/DAY | 0 | 150 | MG | QD | ||||||||
127802262 | 12780226 | 5 | C | METOPROLOL. | METOPROLOL | 1 | 25 MG, 1X/DAY(AT NIGHT) | 0 | 25 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127802262 | 12780226 | 1 | Liver transplant |
127802262 | 12780226 | 3 | Gastrooesophageal reflux disease |
127802262 | 12780226 | 4 | Gout |
127802262 | 12780226 | 5 | Blood pressure abnormal |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127802262 | 12780226 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127802262 | 12780226 | Asthenia | |
127802262 | 12780226 | Blood sodium decreased | |
127802262 | 12780226 | Confusional state | |
127802262 | 12780226 | Disturbance in attention | |
127802262 | 12780226 | Dyspnoea | |
127802262 | 12780226 | Intentional product use issue | |
127802262 | 12780226 | Pericardial effusion | |
127802262 | 12780226 | Product use issue | |
127802262 | 12780226 | Tooth infection |
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 |
---|---|---|---|---|---|---|
127802262 | 12780226 | 1 | 2005 | 0 | ||
127802262 | 12780226 | 2 | 20160916 | 0 | ||
127802262 | 12780226 | 4 | 2009 | 0 |