Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810393 | 6124932 | F | 6810393-3 | 20010501 | 20100616 | 20100630 | EXP | PHEH2006US11227 | NOVARTIS PHARMACEUTICAL CORPORATION | 54 | YR | F | Y | 77.551 | KG | 20100630 | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810393 | 1014007701 | PS | ZOMETA | 1 | INTRAVENOUS | 4MG IV EVERY 4 WEEKS | 021223 | ||||
| 6810393 | 1014007702 | C | EFFEXOR | 1 | 75 MG, TID | ||||||
| 6810393 | 1014007703 | C | VERAPAMIL | 2 | 240 MG, QD | ||||||
| 6810393 | 1014007704 | C | LEXAPRO | 1 | |||||||
| 6810393 | 1014007705 | C | PERCOCET | 1 | |||||||
| 6810393 | 1014007706 | C | PRILOSEC | 1 | |||||||
| 6810393 | 1014007707 | C | DICLOFENAC SODIUM | 1 | |||||||
| 6810393 | 1014007708 | C | NORTRIPTYLINE | 2 | |||||||
| 6810393 | 1014007709 | C | WELLBUTRIN | 1 | |||||||
| 6810393 | 1014007710 | C | KLONOPIN | 1 | |||||||
| 6810393 | 1014007711 | C | ATIVAN | 1 | |||||||
| 6810393 | 1014007712 | C | VITAMIN B-12 | 1 | |||||||
| 6810393 | 1014007713 | C | DOXYCYCLINE | 1 | |||||||
| 6810393 | 1014007714 | C | ADVIL LIQUI-GELS | 1 | |||||||
| 6810393 | 1014007715 | C | CALCIUM WITH VITAMIN D | 2 | |||||||
| 6810393 | 1014007716 | C | STEROIDS NOS | 2 | |||||||
| 6810393 | 1014007717 | C | ZYRTEC | 1 | |||||||
| 6810393 | 1014007718 | C | MOTRIN | 1 | |||||||
| 6810393 | 1014007719 | C | AMOXIL ^AYERST LAB^ | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6810393 | 1014007703 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6810393 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6810393 | ACTINOMYCOSIS |
| 6810393 | ANXIETY |
| 6810393 | ARTHRALGIA |
| 6810393 | ARTHRITIS |
| 6810393 | BARRETT'S OESOPHAGUS |
| 6810393 | BONE DISORDER |
| 6810393 | BREAST TENDERNESS |
| 6810393 | CHRONIC OBSTRUCTIVE PULMONARY DISEASE |
| 6810393 | DECREASED INTEREST |
| 6810393 | DENTAL CARE |
| 6810393 | DIARRHOEA |
| 6810393 | EAR PAIN |
| 6810393 | ERYTHEMA |
| 6810393 | FACIAL PAIN |
| 6810393 | GASTROINTESTINAL HAEMORRHAGE |
| 6810393 | GENERAL PHYSICAL HEALTH DETERIORATION |
| 6810393 | GINGIVAL DISORDER |
| 6810393 | GINGIVAL OPERATION |
| 6810393 | HYPOAESTHESIA |
| 6810393 | IMPAIRED WORK ABILITY |
| 6810393 | JAW OPERATION |
| 6810393 | LIBIDO DECREASED |
| 6810393 | LYMPHADENOPATHY |
| 6810393 | MUCOSAL ULCERATION |
| 6810393 | MULTIPLE MYELOMA |
| 6810393 | MYALGIA |
| 6810393 | NEUROPATHY PERIPHERAL |
| 6810393 | ORAL DISORDER |
| 6810393 | ORAL INFECTION |
| 6810393 | OSTEOMYELITIS |
| 6810393 | OSTEONECROSIS OF JAW |
| 6810393 | OSTEOSCLEROSIS |
| 6810393 | PAIN |
| 6810393 | PARAESTHESIA |
| 6810393 | PERIODONTAL DESTRUCTION |
| 6810393 | PERIODONTITIS |
| 6810393 | PHARYNGEAL OEDEMA |
| 6810393 | RASH |
| 6810393 | RESTLESS LEGS SYNDROME |
| 6810393 | SLEEP APNOEA SYNDROME |
| 6810393 | SOFT TISSUE DISORDER |
| 6810393 | SPINAL OSTEOARTHRITIS |
| 6810393 | SWELLING |
| 6810393 | TENDERNESS |
| 6810393 | TOOTH ABSCESS |
| 6810393 | TOOTH DEPOSIT |
| 6810393 | TOOTH DISORDER |
| 6810393 | TOOTH EXTRACTION |
| 6810393 | TOOTH LOSS |
| 6810393 | VITAMIN B12 DEFICIENCY |
| 6810393 | VULVOVAGINAL DRYNESS |
| 6810393 | WOUND DEHISCENCE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6810393 | 1014007701 | 20050926 |