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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122400463 | 12240046 | 3 | F | 20160115 | 20160816 | 20160405 | 20160822 | PER | PHHY2016US042656 | NOVARTIS | 42.78 | YR | F | Y | 131.52000 | KG | 20160822 | OT | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122400463 | 12240046 | 1 | PS | GILENYA | FINGOLIMOD HYDROCHLORIDE | 1 | Oral | UNK, QD | U | 22527 | CAPSULE | QD | |||||||
| 122400463 | 12240046 | 2 | C | LASIX | FUROSEMIDE | 1 | Oral | 40 MG, QD | 0 | 40 | MG | TABLET | QD | ||||||
| 122400463 | 12240046 | 3 | C | ADIPEX-P | PHENTERMINE HYDROCHLORIDE | 1 | Oral | 37.5 MG, QD | 0 | 37.5 | MG | TABLET | QD | ||||||
| 122400463 | 12240046 | 4 | C | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Oral | HYDROCODONE BITARTRATE 7.5 MG/ PARACETAMOL 325 MG (1 TABLET EVERY 4 HOURS AS NEEDED) | 0 | 1 | DF | TABLET | |||||||
| 122400463 | 12240046 | 5 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | Oral | 1 DF, BID | 0 | 1 | DF | CAPSULE | BID | ||||||
| 122400463 | 12240046 | 6 | C | XANAX | ALPRAZOLAM | 1 | Oral | 1 MG, 1 TABLET EVERY 8 HOURS AS NEEDED | U | 0 | 1 | DF | TABLET | ||||||
| 122400463 | 12240046 | 7 | C | CATAPRES | CLONIDINE HYDROCHLORIDE | 1 | Oral | 0.1 MG, AT BED TIME | U | 0 | .1 | MG | TABLET | QD | |||||
| 122400463 | 12240046 | 8 | C | PHENERGAN | PROMETHAZINE HYDROCHLORIDE | 1 | Oral | 50 MG, 1 TABLET EVERY 6 HOURS AS NEEDED | U | 0 | 1 | DF | TABLET | ||||||
| 122400463 | 12240046 | 9 | C | TOPAMAX | TOPIRAMATE | 1 | Unknown | 1 TABLET IN THE MORNING AND TWO TABLETS IN THE EVENING | U | 0 | TABLET | BID | |||||||
| 122400463 | 12240046 | 10 | C | NEURONTIN | GABAPENTIN | 1 | Oral | 1 DF, TID | U | 0 | 1 | DF | TABLET | TID | |||||
| 122400463 | 12240046 | 11 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | 40 MG, BID | U | 0 | 40 | MG | CAPSULE | BID | |||||
| 122400463 | 12240046 | 12 | C | VALTREX | VALACYCLOVIR HYDROCHLORIDE | 1 | Oral | 1 G, QD | U | 0 | 1 | G | TABLET | QD | |||||
| 122400463 | 12240046 | 13 | C | PSYLLIUM | PLANTAGO SEED | 1 | Oral | 1 PACKET, QD | U | 0 | 1 | DF | QD | ||||||
| 122400463 | 12240046 | 14 | C | ZANAFLEX | TIZANIDINE HYDROCHLORIDE | 1 | Oral | 4 MG, QD (AT BED TIME) | U | 0 | 4 | MG | TABLET | QD | |||||
| 122400463 | 12240046 | 15 | C | ALBUTEROL SULFATE. | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 2 PUFFS AS NEEDED, EVERY 4 TO 6 HOURS | U | 0 | 2 | DF | INHALER |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122400463 | 12240046 | 1 | Relapsing-remitting multiple sclerosis |
| 122400463 | 12240046 | 2 | Product used for unknown indication |
| 122400463 | 12240046 | 3 | Product used for unknown indication |
| 122400463 | 12240046 | 4 | Pain |
| 122400463 | 12240046 | 5 | Product used for unknown indication |
| 122400463 | 12240046 | 6 | Product used for unknown indication |
| 122400463 | 12240046 | 7 | Product used for unknown indication |
| 122400463 | 12240046 | 8 | Product used for unknown indication |
| 122400463 | 12240046 | 9 | Product used for unknown indication |
| 122400463 | 12240046 | 10 | Product used for unknown indication |
| 122400463 | 12240046 | 11 | Product used for unknown indication |
| 122400463 | 12240046 | 12 | Product used for unknown indication |
| 122400463 | 12240046 | 13 | Product used for unknown indication |
| 122400463 | 12240046 | 14 | Product used for unknown indication |
| 122400463 | 12240046 | 15 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122400463 | 12240046 | OT |
| 122400463 | 12240046 | HO |
| 122400463 | 12240046 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122400463 | 12240046 | Asthenia | |
| 122400463 | 12240046 | Blood glucose increased | |
| 122400463 | 12240046 | Confusional state | |
| 122400463 | 12240046 | Disorientation | |
| 122400463 | 12240046 | Fall | |
| 122400463 | 12240046 | Gait disturbance | |
| 122400463 | 12240046 | Heart rate decreased | |
| 122400463 | 12240046 | Hemiparesis | |
| 122400463 | 12240046 | Hypoaesthesia | |
| 122400463 | 12240046 | Incoherent | |
| 122400463 | 12240046 | Intervertebral disc degeneration | |
| 122400463 | 12240046 | Intervertebral disc disorder | |
| 122400463 | 12240046 | Multiple sclerosis relapse | |
| 122400463 | 12240046 | Muscular weakness | |
| 122400463 | 12240046 | Pain | |
| 122400463 | 12240046 | Pain in extremity | |
| 122400463 | 12240046 | Paraesthesia | |
| 122400463 | 12240046 | Spinal compression fracture | |
| 122400463 | 12240046 | Visual impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |