The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
7023065 6755576 F 7023065-X 20030101 20100916 20100930 EXP PHEH2008US08054 NOVARTIS PHARMACEUTICAL CORPORATION 46 YR M Y 20100930 OT 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
7023065 1014812477 PS ZOMETA 1 INTRAVENOUS 4 MG, QMO 021223
7023065 1014812478 C LUPRON 1
7023065 1014812479 C HYDROCODONE 2
7023065 1014812480 C PEPCID 1
7023065 1014812481 C CASODEX 1 UNK
7023065 1014812482 C LORAZEPAM 2
7023065 1014812483 C NIZORAL 1 UNK
7023065 1014812484 C POTASSIUM CITRATE 1 ONE TABLET B.I.D.
7023065 1014812485 C URISED 2 UNK
7023065 1014812486 C SEPTRA 1 UNK
7023065 1014812487 C VICODIN 1
7023065 1014812488 C FLONASE 1
7023065 1014812489 C KETOCONAZOLE 2 UNK
7023065 1014812490 C PREMARIN 1 UNK
7023065 1014812491 C DURAGESIC-100 1
7023065 1014812492 C OXYCODONE HCL AND ACETAMINOPHEN 1 5-325MG
7023065 1014812493 C TRIAZOLAM 1 0.25 MG
7023065 1014812494 C RADIATION 2
7023065 1014812495 C EPOGEN 1
7023065 1014812496 C MARINOL 1
7023065 1014812497 C PROCRIT /00909301/ 2
7023065 1014812498 C BEXTRA 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7023065 1014812477 PROPHYLAXIS
7023065 1014812491 BONE PAIN

Outcome of event

Event ID OUTC COD
7023065 DS
7023065 OT

Reactions reported

Event ID PT
7023065 ABDOMINAL PAIN
7023065 ABSCESS DRAINAGE
7023065 ADRENAL NEOPLASM
7023065 ANAEMIA
7023065 ANHEDONIA
7023065 ANXIETY
7023065 BACK PAIN
7023065 BILIARY CYST
7023065 BLADDER CALCULUS REMOVAL
7023065 BLADDER HYPERTROPHY
7023065 BLOOD TESTOSTERONE DECREASED
7023065 BLOOD URINE PRESENT
7023065 BONE DENSITY DECREASED
7023065 BONE DISORDER
7023065 BONE PAIN
7023065 BREAST TENDERNESS
7023065 CALCULUS BLADDER
7023065 CHILLS
7023065 COLITIS
7023065 CONCOMITANT DISEASE PROGRESSION
7023065 CONSTIPATION
7023065 DEBRIDEMENT
7023065 DENTAL DISCOMFORT
7023065 DYSPNOEA
7023065 DYSURIA
7023065 FATIGUE
7023065 GAIT DISTURBANCE
7023065 GINGIVAL BLEEDING
7023065 GINGIVAL EROSION
7023065 GINGIVAL OEDEMA
7023065 GINGIVITIS
7023065 GYNAECOMASTIA
7023065 HAEMATURIA
7023065 HOT FLUSH
7023065 INFECTION
7023065 INJURY
7023065 INSOMNIA
7023065 INTESTINAL FUNCTIONAL DISORDER
7023065 LUNG NEOPLASM
7023065 MENTAL DISORDER
7023065 NAUSEA
7023065 NECK PAIN
7023065 NEPHROLITHIASIS
7023065 NIGHT SWEATS
7023065 NOCTURIA
7023065 OPEN WOUND
7023065 OSTEONECROSIS OF JAW
7023065 PAIN
7023065 PAIN IN JAW
7023065 PELVIC PAIN
7023065 PERIODONTITIS
7023065 PROSTATE CANCER METASTATIC
7023065 PROSTATIC SPECIFIC ANTIGEN INCREASED
7023065 SEBORRHOEIC KERATOSIS
7023065 SWELLING
7023065 TENDON OPERATION
7023065 TOOTH EXTRACTION
7023065 TOOTH FRACTURE

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
7023065 1014812477 20030423 20070601
7023065 1014812481 20060101
7023065 1014812489 20061001 20070101
7023065 1014812490 20070101