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BONE SCAN ABNORMAL side effect

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Aredia Side Effects Report #5589279-0
Consumer or non-health professional from FRANCE reported AREDIA problem on Jan 04, 2008. Male patient, 75 years of age, was diagnosed with pathological fracture, rheumatoid arthritis and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, face and mouth x-ray abnormal, granuloma, lymphadenopathy, osteolysis, osteonecrosis, pain in jaw, . AREDIA dosage: unknown. During the same period patient was treated with FOSAMAX PLUS D, CORTANCYL, METHOTREXATE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5576925-0
HUMIRA problem was reported by a Consumer or non-health professional from BRAZIL on Dec 20, 2007. Female patient, weighting 134.5 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, oedema peripheral, pain, pyrexia, . HUMIRA dosage: unknown. During the same period patient was treated with MAGISTRALMULA WITH CORTICOID AND ANTI, AMLODIPINE BESYLATE, DIUPRES, SERTRALINE. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5461133-4
Pharmacist from AUSTRALIA reported ZOMETA problem on Sept 17, 2007. Female patient, 58 years of age, was diagnosed with breast cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, dysaesthesia, impaired healing, jaw fracture, osteonecrosis, pain in jaw, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with TAXOL, GEMCITABINE, PAMIDRONATE DI. Patient recovered.

Zometa Side Effects Report #5463964-3
ZOMETA problem was reported by a Physician from UNITED STATES on Sept 14, 2007. Female patient was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, pain in jaw, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with TARCEVA. Patient recovered.


Fentanyl Side Effects Report #5389072-8
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on July 06, 2007. Female patient, weighting 120.0 lb, was diagnosed with paraesthesia, burning sensation, nervousness and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, CLONAZEPAM, CYMBALTA. Patient recovered.

Boniva Side Effects Report #5392441-3
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2007. Female patient, 54 years of age, was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, constipation, diarrhoea, ileal perforation, influenza, . BONIVA dosage: unknown. During the same period patient was treated with KEFLEX, RANITIDINE, FLONASE, FLOVENT, SPIRIVA, TYLENOL, ASPIRIN. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5389072-8
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on July 06, 2007. Female patient, weighting 120.0 lb, was diagnosed with paraesthesia, burning sensation, nervousness and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, CLONAZEPAM, CYMBALTA. Patient recovered.

Boniva Side Effects Report #5392441-3
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2007. Female patient, 54 years of age, was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, constipation, diarrhoea, ileal perforation, influenza, . BONIVA dosage: unknown. During the same period patient was treated with KEFLEX, RANITIDINE, FLONASE, FLOVENT, SPIRIVA, TYLENOL, ASPIRIN. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5787535-4
Pharmacist from UNITED STATES reported BONIVA problem on June 17, 2008. Female patient, 45 years of age, was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, . BONIVA dosage: unknown. Patient recovered.


Revlimid Side Effects Report #5794318-8
REVLIMID problem was reported by a Physician from UNITED STATES on June 17, 2008. Female patient, 79 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, chest pain, malaise, neuralgia, platelet count decreased, pleurisy, . REVLIMID dosage: 15 MG, DAILY X 28 DAYS, ORAL, 15 MG, DAILY X 28 DAYS. Patient was hospitalized and became disabled. Patient recovered.

Teriparatide Side Effects Report #5700227-2
Consumer or non-health professional from UNITED STATES reported TERIPARATIDE problem on Mar 27, 2008. Female patient, weighting 144.0 lb, was diagnosed with osteoporosis and was treated with TERIPARATIDE. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, . TERIPARATIDE dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN D. Patient recovered.

Revlimid Side Effects Report #5725735-X
REVLIMID problem was reported by a Pharmacist from UNITED STATES on Apr 15, 2008. Female patient, 79 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, chest pain, malaise, neuralgia, platelet count decreased, pleurisy, . REVLIMID dosage: 15 MG, DAILY X 28 DAYS, ORAL. Patient was hospitalized and became disabled. Patient recovered.

Betaseron Side Effects Report #5370904-4
Physician from UNITED STATES reported BETASERON problem on June 11, 2007. Female patient, 53 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, injection site abscess, intervertebral disc protrusion, nuclear magnetic resonance imaging abnormal, pain, spinal cord disorder, . BETASERON dosage: unknown. During the same period patient was treated with CORTICOSTEROIDS. Patient recovered.

Omniscan Side Effects Report #5375650-9
OMNISCAN problem was reported by a Physician from CANADA on June 19, 2007. Female patient was diagnosed with aortic aneurysm and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, nephrogenic fibrosing dermopathy, pain in extremity, . OMNISCAN dosage: unknown. Patient recovered.


Zometa Side Effects Report #5256009-1
Physician from KOREA, REPUBLIC OF reported ZOMETA problem on Feb 23, 2007. Female patient, 39 years of age, was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, metastases to bone, osteonecrosis, pain in jaw, . ZOMETA dosage: unknown. Patient recovered.

Voltaren Side Effects Report #5261828-1
VOLTAREN problem was reported by a Consumer or non-health professional from AUSTRALIA on Feb 28, 2007. Male patient, 79 years of age, was diagnosed with bone disorder and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, fall, impaired healing, tooth extraction, . VOLTAREN dosage: unknown. During the same period patient was treated with FOSAMAX. Patient recovered.

Zometa Side Effects Report #5264521-4
Physician from IRELAND reported ZOMETA problem on Mar 05, 2007. Male patient was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, osteonecrosis, pain in jaw, purulent discharge, tooth extraction, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with ANTIINFLAMMATORY, ANTIBIOTICS. Patient recovered.

Voltaren Side Effects Report #5264769-9
VOLTAREN problem was reported by a Consumer or non-health professional from AUSTRALIA on Feb 28, 2007. Male patient, 79 years of age, was diagnosed with bone disorder and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: bone scan abnormal, fall, impaired healing, tooth extraction, . VOLTAREN dosage: unknown. During the same period patient was treated with FOSAMAX. Patient recovered.

Zoledronic Side Effects Report #5614992-6
Physician from UNITED STATES reported ZOLEDRONIC ACID problem on Jan 29, 2008. Female patient, 54 years of age, was diagnosed with metastases to bone, breast cancer and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: biopsy bone abnormal, bone scan abnormal, osteonecrosis, positron emission tomogram abnormal, . ZOLEDRONIC ACID dosage: unknown. Patient recovered.


Ibuprofen Side Effects Report #5506745-4
IBUPROFEN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 05, 2007. Male patient, 49 years of age, was diagnosed with pain and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, bone scan abnormal, endocarditis staphylococcal, osteomyelitis, . IBUPROFEN dosage: unknown. During the same period patient was treated with VOLTAREN. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5490520-3
Physician from NETHERLANDS reported HUMIRA problem on Oct 17, 2007. Female patient, weighting 165.3 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthritis bacterial, bone scan abnormal, cholelithiasis, colitis, listeriosis, malaise, nausea, osteoporosis, skin candida, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISOLONE, NAPROXEN, ALENDRONINE ACID PCH. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5401717-2
FORTEO problem was reported by a Physician from UNITED STATES on July 18, 2007. Female patient, 49 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: back pain, bone scan abnormal, primitive neuroectodermal tumour, . FORTEO dosage: unknown. Patient recovered.

Forteo Side Effects Report #5401717-2
Physician from UNITED STATES reported FORTEO problem on July 18, 2007. Female patient, 49 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: back pain, bone scan abnormal, primitive neuroectodermal tumour, . FORTEO dosage: unknown. Patient recovered.

Forteo Side Effects Report #5704837-8
FORTEO problem was reported by a Physician from UNITED STATES on Apr 03, 2008. Female patient, 49 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: back pain, bone scan abnormal, primitive neuroectodermal tumour, . FORTEO dosage: unknown. Patient recovered.

Zometa Side Effects Report #5683956-9
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Mar 19, 2008. Female patient, 50 years of age, weighting 136.0 lb, was diagnosed with hypercalcaemia of malignancy, cardiomyopathy, pain and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy bone abnormal, bone scan abnormal, calculus ureteric, debridement, dental implantation, dysuria, fistula, flank pain, . ZOMETA dosage: 4 MG MONTHLY. During the same period patient was treated with LANOXIN, CELEBREX, PREVACID, IBUPROFEN. Patient was hospitalized. Patient recovered.

Alendronic Side Effects Report #5648362-1
ALENDRONIC ACID problem was reported by a Consumer or non-health professional from HONG KONG on Feb 18, 2008. Female patient, 82 years of age, was diagnosed with osteoporosis and was treated with ALENDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: blood parathyroid hormone increased, bone lesion, bone scan abnormal, creatinine renal clearance decreased, fall, femur fracture, hydroxyproline increased, low turnover osteopathy, pain in extremity, . ALENDRONIC ACID dosage: 70 MG WEEKLY ORAL. During the same period patient was treated with GLUCOSAMINE HYDROCHLORIDE, CHONDROITIN SULPHATE, CALCIUM CARBONATE, VITAMIN D. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5541658-3
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Dec 03, 2007. Female patient, 60 years of age, weighting 240.0 lb, was diagnosed with breast cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anxiety, bone density decreased, bone scan abnormal, breast cancer metastatic, dyspnoea, injury, metastases to bone, musculoskeletal chest pain, nephrolithiasis, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with FEMARA, AREDIA, PROVENTIL, PAXIL, DARVOCET, AROMASIN. Patient recovered.

Zometa Side Effects Report #5427070-6
ZOMETA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient, 50 years of age, weighting 136.0 lb, was diagnosed with cardiomyopathy and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy bone abnormal, bone scan abnormal, calculus ureteric, dental implantation, dysuria, flank pain, hydronephrosis, impaired healing, . ZOMETA dosage: 4 MG MONTHLY. During the same period patient was treated with LANOXIN, CELEBREX, PREVACID. Patient recovered.

Aredia Side Effects Report #5427167-0
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Aug 20, 2007. Male patient, 51 years of age, weighting 154.0 lb, was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: biopsy bone abnormal, biopsy peripheral nerve, bone scan abnormal, edentulous, gingival erosion, gingival pain, hypoaesthesia, . AREDIA dosage: 90 MG, QMO. During the same period patient was treated with ZOMETA, WARFARIN, FAMVIR, ALEVE, NEURONTIN. Patient recovered.

Zometa Side Effects Report #5743561-2
ZOMETA problem was reported by a Consumer or non-health professional from UNITED STATES on May 09, 2008. Female patient, 50 years of age, weighting 136.0 lb, was diagnosed with hypercalcaemia of malignancy, cardiomyopathy, pain and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy bone abnormal, bone scan abnormal, calculus ureteric, cellulitis, culture positive, dental caries, dental implantation, dysuria, . ZOMETA dosage: 4 MG MONTHLY. During the same period patient was treated with LANOXIN, CELEBREX, PREVACID, IBUPROFEN. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5703717-1
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Apr 07, 2008. Female patient, 60 years of age, weighting 245.0 lb, was diagnosed with breast cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anxiety, bone density decreased, bone scan abnormal, breast cancer metastatic, dyspnoea, injury, metastases to bone, musculoskeletal chest pain, nephrolithiasis, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with FEMARA, AREDIA, PROVENTIL, PAXIL, DARVOCET, AROMASIN. Patient recovered.

Arimidex Side Effects Report #5257672-1
ARIMIDEX problem was reported by a Consumer or non-health professional from CANADA on Jan 29, 2007. Female patient, 67 years of age, was diagnosed with breast cancer female and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: abnormal sensation in eye, arthropathy, bone scan abnormal, dizziness, eyelid ptosis, headache, nausea, pain, paraesthesia, . ARIMIDEX dosage: unknown. During the same period patient was treated with SYNTHROID. Patient recovered.

Decadron Side Effects Report #5263568-1
Consumer or non-health professional from UNITED STATES reported DECADRON # problem on Mar 08, 2007. Female patient, 52 years of age, weighting 178.0 lb, was diagnosed with metastases to bone and was treated with DECADRON #. After drug was administered, patient experienced the following problems/side effects: anaemia, bone disorder, bone scan abnormal, chest tube insertion, disorientation, dyspnoea, fatigue, gingival pain, . DECADRON # dosage: 10 MG, UNK. During the same period patient was treated with ARANESP, XELODA, MITOXANTRONE, COUMADIN, ADALAT, DIOVAN, ZOLOFT. Patient was hospitalized. Patient died.

Lipitor Side Effects Report #5267735-2
LIPITOR problem was reported by a Physician from BELGIUM on Mar 08, 2007. Male patient, weighting 233.7 lb, was diagnosed with hypercholesterolaemia, hypertension and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, ammonia increased, bone scan abnormal, confusional state, dyspnoea, endocarditis, erythema, fatigue, haemolytic anaemia, . LIPITOR dosage: unknown. During the same period patient was treated with AMLODIPINE, CARVEDILOL, CORTICOSTEROIDS, AUGMENTIN. Patient died on 01/29/2007.

Decadron Side Effects Report #5278212-7
Consumer or non-health professional from UNITED STATES reported DECADRON # problem on Mar 23, 2007. Female patient, 52 years of age, weighting 178.0 lb, was diagnosed with metastases to bone and was treated with DECADRON #. After drug was administered, patient experienced the following problems/side effects: anaemia, bone disorder, bone scan abnormal, chest tube insertion, disorientation, dyspnoea, fatigue, gingival pain, . DECADRON # dosage: 10 MG, UNK. During the same period patient was treated with ARANESP, XELODA, MITOXANTRONE, COUMADIN, ADALAT, DIOVAN, ZOLOFT. Patient was hospitalized. Patient died.