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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127354921 | 12735492 | 1 | I | 20160701 | 20160907 | 20160913 | 20160913 | EXP | GB-MHRA-EYC 00144634 | GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK024208 | GLENMARK | 0.00 | Y | 0.00000 | 20160913 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127354921 | 12735492 | 1 | PS | MONTELUKAST SODIUM. | MONTELUKAST SODIUM | 1 | Oral | 10 MG, OD | U | 90926 | 10 | MG | QD | ||||||
127354921 | 12735492 | 2 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Oral | UNK | U | 0 | |||||||||
127354921 | 12735492 | 3 | C | ASACOL | MESALAMINE | 1 | Unknown | UNK | 0 | ||||||||||
127354921 | 12735492 | 4 | C | BECLOMETHASONE DIPROPIONATE /00212602/ | BECLOMETHASONE DIPROPIONATE | 1 | Nasal | UNK | 0 | ||||||||||
127354921 | 12735492 | 5 | C | CETIRIZINE | CETIRIZINE HYDROCHLORIDE | 1 | Unknown | UNK | 0 | ||||||||||
127354921 | 12735492 | 6 | C | CETRABEN /01690401/ | 2 | Unknown | UNK | 0 | CREAM | ||||||||||
127354921 | 12735492 | 7 | C | COCODAMOL | ACETAMINOPHENCODEINE PHOSPHATE | 1 | Unknown | UNK, PRN | 0 | ||||||||||
127354921 | 12735492 | 8 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | UNK | 0 | ||||||||||
127354921 | 12735492 | 9 | C | GABAPENTIN. | GABAPENTIN | 1 | Unknown | UNK | 0 | ||||||||||
127354921 | 12735492 | 10 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | UNK | 0 | ||||||||||
127354921 | 12735492 | 11 | C | SALBUTAMOL | ALBUTEROL | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127354921 | 12735492 | 1 | Asthma |
127354921 | 12735492 | 2 | Product used for unknown indication |
127354921 | 12735492 | 3 | Product used for unknown indication |
127354921 | 12735492 | 4 | Product used for unknown indication |
127354921 | 12735492 | 5 | Product used for unknown indication |
127354921 | 12735492 | 6 | Product used for unknown indication |
127354921 | 12735492 | 7 | Product used for unknown indication |
127354921 | 12735492 | 8 | Product used for unknown indication |
127354921 | 12735492 | 9 | Product used for unknown indication |
127354921 | 12735492 | 10 | Product used for unknown indication |
127354921 | 12735492 | 11 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127354921 | 12735492 | DE |
127354921 | 12735492 | HO |
127354921 | 12735492 | LT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127354921 | 12735492 | Dyspnoea | |
127354921 | 12735492 | Eosinophilic granulomatosis with polyangiitis | |
127354921 | 12735492 | Malaise |
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 |
---|---|---|---|---|---|---|
127354921 | 12735492 | 1 | 201601 | 0 | ||
127354921 | 12735492 | 2 | 201606 | 0 |