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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8016614 | 8317505 | I | 8016614-6 | 20111215 | 20111226 | 20111231 | EXP | CHPA2011FR018174 | NOVARTIS CONSUMER HEALTH, INC. | 56 | YR | F | Y | 20111231 | CN | FRANCE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8016614 | 1018419879 | PS | SCOPOLAMINE | 1 | TRANSDERMAL | 1 DF, Q72H | 017874 | ||||
8016614 | 1018419880 | SS | SCOPOLAMINE | 1 | TRANSDERMAL | UNK, UNK | 017874 | ||||
8016614 | 1018419882 | C | ESTREVA | 2 | |||||||
8016614 | 1018419881 | C | LEVOTHYROXINE SODIUM | 1 | |||||||
8016614 | 1018419883 | C | PROGESTERONE | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8016614 | 1018419879 | MOTION SICKNESS |
Outcome of event
Event ID | OUTC COD |
---|---|
8016614 | OT |
Reactions reported
Event ID | PT |
---|---|
8016614 | NAUSEA |
8016614 | HEADACHE |
8016614 | VISUAL IMPAIRMENT |
8016614 | VERTIGO |
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 |
---|---|---|---|---|---|
8016614 | 1018419879 | 20111108 | 20111215 | 30 | DAY |
8016614 | 1018419880 | 20080101 | 8 | DAY |