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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125780081 | 12578008 | 1 | I | 2014 | 20160718 | 20160721 | 20160721 | EXP | GB-MHRA-EYC 00142405 | GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK023668 | GLENMARK | 0.00 | Y | 0.00000 | 20160721 | CN | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125780081 | 12578008 | 1 | PS | MONTELUKAST SODIUM. | MONTELUKAST SODIUM | 1 | Oral | 10 MG, HS, INSTRUCTED TO TAKE IN EVENING OR NIGHT BEFORE BED | Y | 90926 | 10 | MG | TABLET | ||||||
125780081 | 12578008 | 2 | C | ACRIVASTINE | ACRIVASTINE | 1 | Unknown | UNK | 0 | ||||||||||
125780081 | 12578008 | 3 | C | CANDESARTAN | CANDESARTAN | 1 | Unknown | UNK | 0 | ||||||||||
125780081 | 12578008 | 4 | C | CODEINE PHOSPHATE | CODEINE PHOSPHATE | 1 | Unknown | UNK | 0 | ||||||||||
125780081 | 12578008 | 5 | C | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Unknown | UNK | 0 | ||||||||||
125780081 | 12578008 | 6 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Unknown | UNK | 0 | ||||||||||
125780081 | 12578008 | 7 | C | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Unknown | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125780081 | 12578008 | 1 | Asthma prophylaxis |
125780081 | 12578008 | 2 | Product used for unknown indication |
125780081 | 12578008 | 3 | Product used for unknown indication |
125780081 | 12578008 | 4 | Product used for unknown indication |
125780081 | 12578008 | 5 | Product used for unknown indication |
125780081 | 12578008 | 6 | Product used for unknown indication |
125780081 | 12578008 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125780081 | 12578008 | DS |
125780081 | 12578008 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125780081 | 12578008 | Anxiety | |
125780081 | 12578008 | Autophobia | |
125780081 | 12578008 | Depression | |
125780081 | 12578008 | Malaise | |
125780081 | 12578008 | Nightmare | |
125780081 | 12578008 | Sleep disorder | |
125780081 | 12578008 | Suicidal ideation |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125780081 | 12578008 | 1 | 2014 | 20160707 | 0 |