Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7915093 | 8245250 | I | 7915093-4 | 20110101 | 20111110 | 20111115 | EXP | US-MERCK-1111USA01437 | MERCK HUMAN HEALTH DIVISION | 28 | YR | F | Y | 20111115 | CN | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
7915093 | 1018050538 | PS | MAXALT-MLT | 1 | ORAL | 020865 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7915093 | 1018050538 | MIGRAINE |
Outcome of event
Event ID | OUTC COD |
---|---|
7915093 | OT |
Reactions reported
Event ID | PT |
---|---|
7915093 | ABORTION SPONTANEOUS |
7915093 | MATERNAL EXPOSURE DURING PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
7915093 | 1018050538 | 20110401 | 20110101 |