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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125607591 | 12560759 | 1 | I | 20160712 | 20160715 | 20160715 | EXP | US-009507513-1607USA005866 | MERCK | 56.00 | YR | M | Y | 0.00000 | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125607591 | 12560759 | 1 | PS | PROVENTIL | ALBUTEROL | 1 | Respiratory (inhalation) | DAILY ALBUTEROL INHALER/AGGRESSIVE ALBUTEROL THERAPY | U | 20503 | INHALATION POWDER | QD | |||||||
| 125607591 | 12560759 | 2 | SS | PROVENTIL | ALBUTEROL | 1 | U | 20503 | INHALATION POWDER | ||||||||||
| 125607591 | 12560759 | 3 | SS | MAGNESIUM SULFATE. | MAGNESIUM SULFATE | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125607591 | 12560759 | 1 | Cough |
| 125607591 | 12560759 | 2 | Respiratory disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125607591 | 12560759 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125607591 | 12560759 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |