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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124953453 | 12495345 | 3 | F | 20160825 | 20160624 | 20160830 | EXP | US-009507513-1606USA009986 | MERCK | 56.00 | YR | F | Y | 0.00000 | 20160830 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124953453 | 12495345 | 1 | PS | PROVENTIL | ALBUTEROL | 1 | Respiratory (inhalation) | 3-4 TIMES DAILY FOR SEVERAL DAYS | Y | 20503 | INHALATION POWDER | ||||||||
124953453 | 12495345 | 2 | SS | PROVENTIL | ALBUTEROL | 1 | Respiratory (inhalation) | 2 ADDITIONAL ROUNDS OF 7.5 MG OF ALBUTEROL (5 MG/ML) | Y | 20503 | 7.5 | MG | INHALATION POWDER | ||||||
124953453 | 12495345 | 3 | SS | METHYLPREDNISOLONE SODIUM SUCCINATE. | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous (not otherwise specified) | 125 MG, UNK | U | 0 | 125 | MG | SOLUTION FOR INJECTION | ||||||
124953453 | 12495345 | 4 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | U | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124953453 | 12495345 | OT |
124953453 | 12495345 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124953453 | 12495345 | Lactic acidosis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |