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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117553272 | 11755327 | 2 | F | 201506 | 20150722 | 20151119 | 20160823 | PER | US-MYLANLABS-2015M1025105 | MYLAN | 72.23 | YR | M | Y | 0.00000 | 20160823 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117553272 | 11755327 | 1 | PS | CLONIDINE TRANSDERMAL SYSTEM | CLONIDINE | 1 | Transdermal | 0.1 MG, QD CHANGE QW | 614178 | 76166 | .1 | MG | TRANSDERMAL PATCH | QD | |||||
| 117553272 | 11755327 | 2 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | UNK | Y | 0 | TABLET | ||||||||
| 117553272 | 11755327 | 3 | C | METOPROLOL. | METOPROLOL | 1 | UNK | U | 0 | ||||||||||
| 117553272 | 11755327 | 4 | C | LISINOPRIL. | LISINOPRIL | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117553272 | 11755327 | 1 | Blood pressure increased |
| 117553272 | 11755327 | 2 | Hypertension |
| 117553272 | 11755327 | 3 | Blood pressure measurement |
| 117553272 | 11755327 | 4 | Blood pressure measurement |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117553272 | 11755327 | Blood pressure fluctuation | |
| 117553272 | 11755327 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |