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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125958281 | 12595828 | 1 | I | 20160708 | 20160720 | 20160726 | 20160726 | EXP | GB-COL_23383_2016 | COLGATE | 40.00 | YR | F | Y | 82.55000 | KG | 20160726 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125958281 | 12595828 | 1 | PS | CHLORHEXIDINE GLUCONATE. | CHLORHEXIDINE GLUCONATE | 1 | Oral | 10ML/2 - 1 DAY/ | Y | U | 1066IE0106 | 73695 | |||||||
125958281 | 12595828 | 2 | C | cosmocol | 2 | NI/NI/ | U | 0 | |||||||||||
125958281 | 12595828 | 3 | C | LACTULOSE. | LACTULOSE | 1 | NI/NI/ | U | 0 | ||||||||||
125958281 | 12595828 | 4 | C | alendronic acid | ALENDRONIC ACID | 1 | NI/NI/ | U | 0 | ||||||||||
125958281 | 12595828 | 5 | SS | cyclizine | CYCLIZINE | 1 | Intramuscular | NI/NI/ | U | U | 0 | ||||||||
125958281 | 12595828 | 6 | C | amitriptyline | AMITRIPTYLINE | 1 | NI/NI/ | U | 0 | ||||||||||
125958281 | 12595828 | 7 | SS | Dihydrocodeine | DIHYDROCODEINE | 1 | NI/NI/ | U | U | 0 | |||||||||
125958281 | 12595828 | 8 | SS | LYRICA | PREGABALIN | 1 | NI/NI/ | U | U | 0 | |||||||||
125958281 | 12595828 | 9 | SS | oramorph | MORPHINE SULFATE | 1 | NI/NI/ | U | U | 0 | |||||||||
125958281 | 12595828 | 10 | C | ADCAL-D3 | CALCIUM CARBONATECHOLECALCIFEROL | 1 | NI/NI/ | U | 0 | ||||||||||
125958281 | 12595828 | 11 | SS | salbutamol | ALBUTEROL | 1 | Respiratory (inhalation) | NI/NI/ | U | U | 0 | ||||||||
125958281 | 12595828 | 12 | SS | SERETIDE | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Respiratory (inhalation) | NI/NI/ | U | U | 0 | ||||||||
125958281 | 12595828 | 13 | SS | LORATADINE. | LORATADINE | 1 | NI/NI/ | U | U | 0 | |||||||||
125958281 | 12595828 | 14 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | NI/NI/ | U | U | 0 | |||||||||
125958281 | 12595828 | 15 | C | MONTELUKAST | MONTELUKAST SODIUM | 1 | NI/NI/ | U | 0 | ||||||||||
125958281 | 12595828 | 16 | C | phenoxymethylpenicillin | PENICILLIN V | 1 | NI/NI/ | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125958281 | 12595828 | 1 | Mouth ulceration |
125958281 | 12595828 | 2 | Product used for unknown indication |
125958281 | 12595828 | 3 | Product used for unknown indication |
125958281 | 12595828 | 4 | Product used for unknown indication |
125958281 | 12595828 | 5 | Product used for unknown indication |
125958281 | 12595828 | 6 | Product used for unknown indication |
125958281 | 12595828 | 7 | Product used for unknown indication |
125958281 | 12595828 | 8 | Product used for unknown indication |
125958281 | 12595828 | 9 | Product used for unknown indication |
125958281 | 12595828 | 10 | Product used for unknown indication |
125958281 | 12595828 | 11 | Product used for unknown indication |
125958281 | 12595828 | 12 | Product used for unknown indication |
125958281 | 12595828 | 13 | Product used for unknown indication |
125958281 | 12595828 | 14 | Product used for unknown indication |
125958281 | 12595828 | 15 | Product used for unknown indication |
125958281 | 12595828 | 16 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125958281 | 12595828 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125958281 | 12595828 | Asthma | |
125958281 | 12595828 | Drug interaction | |
125958281 | 12595828 | Feeling abnormal | |
125958281 | 12595828 | Feeling drunk | |
125958281 | 12595828 | Oral discomfort | |
125958281 | 12595828 | Oxygen saturation decreased | |
125958281 | 12595828 | Swelling face |
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 |
---|---|---|---|---|---|---|
125958281 | 12595828 | 1 | 20160708 | 20160708 | 0 |