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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126347353 | 12634735 | 3 | F | 20160817 | 20160808 | 20160829 | PER | US-PFIZER INC-2016376126 | PFIZER | 69.00 | YR | M | Y | 77.11000 | KG | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126347353 | 12634735 | 1 | PS | ALTACE | RAMIPRIL | 1 | Oral | 5 MG, 1X/DAY (IN THE MORNING) | 19901 | 5 | MG | CAPSULE | QD | ||||||
126347353 | 12634735 | 2 | SS | ALTACE | RAMIPRIL | 1 | Oral | 5 MG, EVERY SECOND DAY | 19901 | 5 | MG | CAPSULE | |||||||
126347353 | 12634735 | 3 | SS | VALIUM | DIAZEPAM | 1 | UNK (AT AN LOW DOSE) | U | 0 | ||||||||||
126347353 | 12634735 | 4 | C | DILTIAZEM. | DILTIAZEM | 1 | UNK (IN THE MORNING) | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126347353 | 12634735 | 1 | Hypertension |
126347353 | 12634735 | 4 | Atrial fibrillation |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126347353 | 12634735 | Dizziness |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |