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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123222407 | 12322240 | 7 | F | 20160421 | 20160915 | 20160502 | 20160923 | EXP | DE-SA-2016SA080913 | AVENTIS | 0.00 | A | F | Y | 97.00000 | KG | 20160923 | OT | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123222407 | 12322240 | 1 | PS | LEMTRADA | ALEMTUZUMAB | 1 | Intravenous drip | EXACT DAILY DOSE NOT INDICATED, ONLY UNIT DOSE?DOSAGE TEXT: 1-0-0 | UNKNOWN | 103948 | 12 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QD | |||||
| 123222407 | 12322240 | 2 | SS | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | DOSAGE; 1-0-0 | UNKNOWN | 0 | 1 | G | QD | ||||||
| 123222407 | 12322240 | 3 | C | RANITIDINE ^RATIOPHARM^ | 2 | Intravenous (not otherwise specified) | DOSAGE: 1-0-0 | 0 | SOLUTION FOR INFUSION | QD | |||||||||
| 123222407 | 12322240 | 4 | C | FAMPYRA | DALFAMPRIDINE | 1 | 0 | BID | |||||||||||
| 123222407 | 12322240 | 5 | C | VESIKUR | SOLIFENACIN SUCCINATE | 1 | 0 | QD | |||||||||||
| 123222407 | 12322240 | 6 | C | TAVEGIL | CLEMASTINE FUMARATE | 1 | Intravenous (not otherwise specified) | DOSAGE TEXT: 1-0-0 | 0 | QD | |||||||||
| 123222407 | 12322240 | 7 | C | TAVANIC | LEVOFLOXACIN | 1 | Oral | DOSAGE TEXT; 1-0-0 | 0 | 500 | MG | TABLET | QD | ||||||
| 123222407 | 12322240 | 8 | C | MAYRA | 2 | Oral | 0 | QD | |||||||||||
| 123222407 | 12322240 | 9 | C | ACICLOVIR | ACYCLOVIR | 1 | 0 | ||||||||||||
| 123222407 | 12322240 | 10 | C | CETIRIZINE | CETIRIZINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 123222407 | 12322240 | 11 | C | PARACETAMOL | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 123222407 | 12322240 | 12 | C | REKAWAN | POTASSIUM CHLORIDE | 1 | 0 | ||||||||||||
| 123222407 | 12322240 | 13 | C | MONO-EMBOLEX | CERTOPARIN SODIUM | 1 | Subcutaneous | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123222407 | 12322240 | 1 | Multiple sclerosis |
| 123222407 | 12322240 | 2 | Prophylaxis |
| 123222407 | 12322240 | 3 | Prophylaxis |
| 123222407 | 12322240 | 5 | Urge incontinence |
| 123222407 | 12322240 | 6 | Prophylaxis |
| 123222407 | 12322240 | 7 | Urinary tract infection |
| 123222407 | 12322240 | 8 | Contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123222407 | 12322240 | DE |
| 123222407 | 12322240 | HO |
| 123222407 | 12322240 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123222407 | 12322240 | Bradycardia | |
| 123222407 | 12322240 | Cerebral haemorrhage | |
| 123222407 | 12322240 | Hypertension | |
| 123222407 | 12322240 | Nausea | |
| 123222407 | 12322240 | Seizure | |
| 123222407 | 12322240 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 123222407 | 12322240 | 1 | 20160418 | 20160420 | 0 | |
| 123222407 | 12322240 | 2 | 20160418 | 20160420 | 0 | |
| 123222407 | 12322240 | 3 | 20160418 | 20160420 | 0 | |
| 123222407 | 12322240 | 6 | 20160418 | 20160420 | 0 | |
| 123222407 | 12322240 | 7 | 20160418 | 20160420 | 0 | |
| 123222407 | 12322240 | 9 | 20160418 | 0 | ||
| 123222407 | 12322240 | 10 | 20160418 | 0 | ||
| 123222407 | 12322240 | 11 | 20160418 | 0 | ||
| 123222407 | 12322240 | 12 | 20160418 | 0 | ||
| 123222407 | 12322240 | 13 | 20160418 | 0 |