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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81426084 | 8142608 | 4 | F | 20100629 | 20160808 | 20110919 | 20160811 | EXP | US-BAYER-2011-084202 | BAYER | 29.00 | YR | A | F | Y | 53.97000 | KG | 20160811 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 81426084 | 8142608 | 1 | PS | YAZ | DROSPIRENONEETHINYL ESTRADIOL | 1 | UNK | 21676 | FILM-COATED TABLET | ||||||||||
| 81426084 | 8142608 | 2 | C | ATIVAN | LORAZEPAM | 1 | 0 | ||||||||||||
| 81426084 | 8142608 | 3 | C | ADVIL | IBUPROFEN | 1 | Oral | AS NEEDED, UNK | 0 | ||||||||||
| 81426084 | 8142608 | 4 | C | IBUPROFEN. | IBUPROFEN | 1 | 0 | ||||||||||||
| 81426084 | 8142608 | 5 | C | DILANTIN | PHENYTOIN | 1 | 0 | ||||||||||||
| 81426084 | 8142608 | 6 | C | KLONOPIN | CLONAZEPAM | 1 | 0 | ||||||||||||
| 81426084 | 8142608 | 7 | C | RITALIN | METHYLPHENIDATE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 81426084 | 8142608 | 8 | C | FENTANYL. | FENTANYL | 1 | 50 MG, UNK | 0 | 50 | MG | |||||||||
| 81426084 | 8142608 | 9 | C | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | 4 MG, PRN | 0 | 4 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 81426084 | 8142608 | 6 | Anxiety |
| 81426084 | 8142608 | 7 | Disturbance in attention |
| 81426084 | 8142608 | 8 | Pain |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 81426084 | 8142608 | DS |
| 81426084 | 8142608 | HO |
| 81426084 | 8142608 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 81426084 | 8142608 | Amnesia | |
| 81426084 | 8142608 | Anhedonia | |
| 81426084 | 8142608 | Anxiety | |
| 81426084 | 8142608 | Aphasia | |
| 81426084 | 8142608 | Arthralgia | |
| 81426084 | 8142608 | Blindness | |
| 81426084 | 8142608 | Burning sensation | |
| 81426084 | 8142608 | Cavernous sinus thrombosis | |
| 81426084 | 8142608 | Cerebrovascular accident | |
| 81426084 | 8142608 | Chest pain | |
| 81426084 | 8142608 | Confusional state | |
| 81426084 | 8142608 | Depression | |
| 81426084 | 8142608 | Disturbance in attention | |
| 81426084 | 8142608 | Dizziness | |
| 81426084 | 8142608 | Encephalopathy | |
| 81426084 | 8142608 | Exercise tolerance decreased | |
| 81426084 | 8142608 | Fatigue | |
| 81426084 | 8142608 | Fear | |
| 81426084 | 8142608 | Gait disturbance | |
| 81426084 | 8142608 | Haemorrhage intracranial | |
| 81426084 | 8142608 | Headache | |
| 81426084 | 8142608 | Hypoaesthesia | |
| 81426084 | 8142608 | Impulsive behaviour | |
| 81426084 | 8142608 | Injury | |
| 81426084 | 8142608 | Memory impairment | |
| 81426084 | 8142608 | Muscle spasms | |
| 81426084 | 8142608 | Muscular weakness | |
| 81426084 | 8142608 | Paraesthesia | |
| 81426084 | 8142608 | Seizure | |
| 81426084 | 8142608 | Sleep disorder | |
| 81426084 | 8142608 | Status epilepticus | |
| 81426084 | 8142608 | Vertigo | |
| 81426084 | 8142608 | Vision blurred |
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 |
|---|---|---|---|---|---|---|
| 81426084 | 8142608 | 1 | 20090402 | 2010 | 0 | |
| 81426084 | 8142608 | 3 | 2000 | 0 |