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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127829211 | 12782921 | 1 | I | 20160920 | 20160927 | 20160927 | PER | US-PFIZER INC-2016443822 | PFIZER | 88.00 | YR | M | Y | 59.41000 | KG | 20160927 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127829211 | 12782921 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | UNK, DAILY (5 QD) | U | 19901 | ||||||||||
127829211 | 12782921 | 2 | SS | RAMIPRIL. | RAMIPRIL | 1 | U | 19901 | |||||||||||
127829211 | 12782921 | 3 | SS | RAMIPRIL. | RAMIPRIL | 1 | U | 19901 | |||||||||||
127829211 | 12782921 | 4 | SS | COREG | CARVEDILOL | 1 | UNK, 2X/DAY (6.25 BID) | U | 0 | BID | |||||||||
127829211 | 12782921 | 5 | SS | COREG | CARVEDILOL | 1 | U | 0 | |||||||||||
127829211 | 12782921 | 6 | SS | COREG | CARVEDILOL | 1 | U | 0 | |||||||||||
127829211 | 12782921 | 7 | SS | LASIX | FUROSEMIDE | 1 | UNK, 2X/DAY (40 BID) | U | 0 | BID | |||||||||
127829211 | 12782921 | 8 | SS | LASIX | FUROSEMIDE | 1 | U | 0 | |||||||||||
127829211 | 12782921 | 9 | SS | LASIX | FUROSEMIDE | 1 | U | 0 | |||||||||||
127829211 | 12782921 | 10 | C | ASA | ASPIRIN | 1 | UNK | 0 | |||||||||||
127829211 | 12782921 | 11 | C | PLAVIX | CLOPIDOGREL BISULFATE | 1 | UNK | 0 | |||||||||||
127829211 | 12782921 | 12 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | UNK | 0 | |||||||||||
127829211 | 12782921 | 13 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127829211 | 12782921 | 1 | Cardiac failure congestive |
127829211 | 12782921 | 2 | Coronary artery disease |
127829211 | 12782921 | 3 | Amyloidosis |
127829211 | 12782921 | 4 | Cardiac failure congestive |
127829211 | 12782921 | 5 | Coronary artery disease |
127829211 | 12782921 | 6 | Amyloidosis |
127829211 | 12782921 | 7 | Cardiac failure congestive |
127829211 | 12782921 | 8 | Coronary artery disease |
127829211 | 12782921 | 9 | Amyloidosis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127829211 | 12782921 | Asthenia | |
127829211 | 12782921 | Dyspnoea | |
127829211 | 12782921 | Faeces discoloured | |
127829211 | 12782921 | Oedema |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |