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Index of reports
> Cases resulting in disability (47)
Below is the selection of adverse event reports related to Aredia (Pamidronate) that includes cases resulting in disability.
Reports 1 - 25 of 47 Next >>
Adverse event in 62 year old male receiving Aredia (Pamidronate)
Reported by a physician from Australia on 2007-10-22
Patient: 62 year old male
Adverse reactions / side effects: Soft Tissue Infection, Osteonecrosis, Surgery, Impaired Healing, Bone Disorder, Oedema Mouth, Pain in JAW
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Zometa
Dosage: 4mg every 3 months
End date: 2006-11-15
Aredia
Dosage: 90mg
Start date: 1998-01-01
Other drugs received by patient: Melphalan; Prednisolone; Morphine; Gabapentin; Aspirin; Lipitor; Valtrex; Mobic; Vincristine + Adriamycin + Dexamethasone
Adverse event in 65 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Japan on 2007-10-10
Patient: 65 year old female, weighing 31.0 kg (68.2 pounds)
Adverse reactions / side effects: Stomatitis, Incisional Drainage, Abscess Oral, Tooth Extraction, Osteomyelitis, Periodontitis, Discomfort, Osteonecrosis, Sequestrectomy, Swelling, Mastectomy, Bone Disorder, Lymphadenectomy, Loose Tooth, Sinusitis, Inflammation
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Aredia (Pamidronate)
Other drugs received by patient: Antineoplastic Agents; Taxotere; Taxotere; Taxotere; Epirubicin HCL; UFT
Adverse event in 60 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from France on 2007-10-08
Patient: 60 year old female
Adverse reactions / side effects: Metastases TO Liver, Radiation Injury, Death, Facial Neuralgia, Musculoskeletal Stiffness, Bone Density Decreased, Bone Disorder, Metastases TO Ovary, Stomatitis, Dysphagia, Mouth Haemorrhage, Paraesthesia, Mucosal Inflammation, Osteosclerosis, Osteonecrosis, Mastication Disorder, Infection, Inflammation
Adverse event resulted in: death, disablity
Suspect drug(s):
Clastoban
Dosage: unk, unk
Administration route: Oral
Indication: Breast Cancer Metastatic
Start date: 1998-03-21
End date: 1999-06-30
Zometa
Indication: Metastases TO Bone
Start date: 2002-09-07
Aredia
Indication: Metastases TO Bone
Start date: 1999-10-27
End date: 2000-01-07
Aredia
Start date: 2002-03-07
End date: 2002-08-21
Other drugs received by patient: Taxotere; Taxotere; Xeloda; Fortimel; Femara; Taxol; Radiotherapy; Navelbine; Epirubicin
Adverse event in 65 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Japan on 2007-10-04
Patient: 65 year old female, weighing 31.0 kg (68.2 pounds)
Adverse reactions / side effects: Stomatitis, Incisional Drainage, Abscess Oral, Tooth Extraction, Osteomyelitis, Discomfort, Osteonecrosis, Sequestrectomy, Swelling, Mastectomy, Loose Tooth, Bone Disorder, Lymphadenectomy, Sinusitis, Inflammation
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Aredia (Pamidronate)
Other drugs received by patient: Antineoplastic Agents; Taxotere; Taxotere; Taxotere; Epirubicin HCL; UFT
Adverse event in 65 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Japan on 2007-10-04
Patient: 65 year old female, weighing 31.0 kg (68.2 pounds)
Adverse reactions / side effects: Tooth Extraction, Osteomyelitis, Sequestrectomy, Lymphadenectomy, Bone Disorder, Sinusitis, Stomatitis, Incisional Drainage, Abscess Oral, Subcutaneous Abscess, Gingival Swelling, Discomfort, Osteonecrosis, Swelling, Mastectomy, Loose Tooth, Inflammation
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Aredia (Pamidronate)
Other drugs received by patient: Antineoplastic Agents; Taxotere; Taxotere; Taxotere; Epirubicin HCL; UFT
Adverse event in 53 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from France on 2007-10-02
Patient: 53 year old female
Adverse reactions / side effects: Back Pain, Aphthous Stomatitis, Cheilitis, Osteonecrosis, Tooth Abscess, Dental Care, Pelvic Pain, Oral Herpes
Adverse event resulted in: disablity
Suspect drug(s):
Zometa
Dosage: 4 mg, tiw
Indication: Metastases TO Bone
Start date: 2004-03-23
End date: 2007-04-23
Aredia
Indication: Metastases TO Bone
Start date: 2002-05-16
End date: 2003-01-07
Lytos
Indication: Metastases TO Bone
Start date: 2002-05-16
End date: 2004-08-09
Endoxan
Indication: Breast Cancer Metastatic
Start date: 2007-02-05
End date: 2007-03-08
Fluorouracil
Indication: Breast Cancer Metastatic
Start date: 2007-02-05
End date: 2007-03-08
Other drugs received by patient: Navelbine; Navelbine; Thiotepa; Thiotepa; Clastoban; Aromasin; Femara; Radiotherapy; Xeloda; Taxotere; Taxotere; Caelyx; Genox; Taxol; Taxol; Carboplatin; Methotrexate
Adverse event in 63 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Japan on 2007-10-02
Patient: 63 year old female
Adverse reactions / side effects: LIP Swelling, Metastases TO Liver, Tooth Extraction, Malignant Neoplasm Progression, Soft Tissue Inflammation, Hepatic Failure, Osteonecrosis, Oral Pain, Anorexia, Bone Disorder
Adverse event resulted in: death, hospitalization, disablity
Suspect drug(s):
Aredia (Pamidronate)
Other drugs received by patient: Paclitaxel; Herceptin; Docetaxel
Adverse event in female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Germany on 2007-07-27
Patient: female
Adverse reactions / side effects: Abscess Drainage, JAW Operation, Tooth Extraction, Abscess JAW, Osteitis, Periodontitis, Antibiotic Prophylaxis, Death, Osteonecrosis, Actinomycosis
Adverse event resulted in: death, disablity
Suspect drug(s):
Aredia
Dosage: 90 mg, unk
Indication: Multiple Myeloma
Start date: 2000-07-01
End date: 2001-06-01
Zometa
Dosage: 4 mg, unk
Indication: Multiple Myeloma
Start date: 2001-07-01
Other drugs received by patient: Aspirin; Furo; Metoprolol Succinate; Dekristol; Digitoxin TAB; Vesdil; Clindamycin HCL
Adverse event in female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Germany on 2007-07-27
Patient: female
Adverse reactions / side effects: Abscess Drainage, JAW Operation, Tooth Extraction, Abscess JAW, Osteitis, Periodontitis, Antibiotic Prophylaxis, Death, Osteonecrosis, Actinomycosis
Adverse event resulted in: death, disablity
Suspect drug(s):
Aredia
Dosage: 90 mg, unk
Indication: Multiple Myeloma
Start date: 2000-07-01
End date: 2001-06-01
Zometa
Dosage: 4 mg, unk
Indication: Multiple Myeloma
Start date: 2001-07-01
Other drugs received by patient: Aspirin; Furo; Metoprolol Succinate; Dekristol; Digitoxin TAB; Vesdil; Clindamycin HCL
Adverse event in female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Germany on 2007-07-27
Patient: female
Adverse reactions / side effects: Abscess Drainage, JAW Operation, Tooth Extraction, Abscess JAW, Osteitis, Periodontitis, Antibiotic Prophylaxis, Death, Osteonecrosis, Actinomycosis
Adverse event resulted in: death, disablity
Suspect drug(s):
Aredia
Dosage: 90 mg, unk
Indication: Multiple Myeloma
Start date: 2000-07-01
End date: 2001-06-01
Zometa
Dosage: 4 mg, unk
Indication: Multiple Myeloma
Start date: 2001-07-01
Other drugs received by patient: Aspirin; Furo; Metoprolol Succinate; Dekristol; Digitoxin TAB; Vesdil; Clindamycin HCL
Adverse event in 53 year old male receiving Aredia (Pamidronate)
Reported by a physician from Germany on 2007-07-20
Patient: 53 year old male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Oral Surgery, Tooth Extraction, Osteomyelitis, Biopsy, Osteonecrosis, Dental Treatment, Abscess, Sinusitis
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Zometa
Dosage: 4 mg, qmo
Indication: Multiple Myeloma
Start date: 2003-10-01
End date: 2005-10-01
Aredia
Dosage: 90 mg qmo
Indication: Multiple Myeloma
Start date: 1998-01-01
End date: 2003-01-01
Adverse event in 65 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from Italy on 2007-07-13
Patient: 65 year old female
Adverse reactions / side effects: Fistula, Osteonecrosis
Adverse event resulted in: disablity
Suspect drug(s):
Zometa
Dosage: 4 mg/month
Indication: Multiple Myeloma
Start date: 1992-01-01
End date: 1997-01-01
Aredia
Dosage: 15 mg/month
Indication: Multiple Myeloma
Start date: 1992-02-01
End date: 1997-01-01
Adverse event in 71 year old male receiving Aredia (Pamidronate)
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-07-13
Patient: 71 year old male
Adverse reactions / side effects: Fistula, Osteonecrosis, Sequestrectomy, Abscess, Bone Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Aredia
Dosage: 90 mg, qmo
Indication: Multiple Myeloma
Start date: 2003-03-17
End date: 2003-08-30
Zometa
Dosage: 4 mg, qmo
Indication: Multiple Myeloma
Start date: 2003-09-18
End date: 2003-10-30
Other drugs received by patient: Alkeran
Adverse event in 72 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from France on 2007-06-25
Patient: 72 year old female
Adverse reactions / side effects: Osteonecrosis, Impaired Healing, Tooth Extraction, Pain in JAW
Adverse event resulted in: disablity
Suspect drug(s):
Zometa
Indication: Multiple Myeloma
Start date: 2006-09-15
Fosamax Once Weekly
Dosage: 1 df, qw
Administration route: Oral
Indication: Osteoporosis
Start date: 2001-07-01
End date: 2006-07-01
Aredia
Dosage: 1 df, qmo
Indication: Multiple Myeloma
Start date: 2006-06-15
End date: 2006-08-15
Adverse event in 65 year old male receiving Aredia (Pamidronate)
Reported by a physician from Australia on 2007-06-11
Patient: 65 year old male
Adverse reactions / side effects: Soft Tissue Infection, Osteonecrosis, Surgery, Impaired Healing, Bone Disorder, Oedema Mouth, Pain in JAW
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Zometa
Dosage: 4mg every 3 months
End date: 2006-10-01
Aredia
Dosage: 90mg
Start date: 1998-01-01
Other drugs received by patient: Melphalan; Prednisolone; Morphine; Gabapentin; Aspirin; Lipitor; Valtrex; Mobic; Vincristine + Adriamycin + Dexamethasone
Adverse event in 47 year old female receiving Aredia (Pamidronate)
Reported by a physician from Australia on 2007-06-08
Patient: 47 year old female
Adverse reactions / side effects: Oral Surgery, Bone Lesion, Tooth Extraction, Soft Tissue Infection, Osteonecrosis, Impaired Healing, Oedema Mouth, Bone Disorder, Dysaesthesia, Pain in JAW
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Zometa
Dosage: 4 mg, q3mo
Indication: Multiple Myeloma
Start date: 2004-01-01
End date: 2006-10-25
Aredia
Indication: Multiple Myeloma
Start date: 1998-01-01
End date: 2004-01-01
Other drugs received by patient: Melphalan; Vincristine + Adriamycin + Dexamethasone; Thalidomide; Steroids NOS
Adverse event in 54 year old male receiving Aredia (Pamidronate)
Reported by a physician from Australia on 2007-06-08
Patient: 54 year old male
Adverse reactions / side effects: Soft Tissue Infection, Oral Surgery, Osteonecrosis, Face Oedema, Bone Lesion, Dysaesthesia, Bone Disorder, Pain in JAW
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Zometa
Indication: Multiple Myeloma
Aredia
Indication: Multiple Myeloma
Other drugs received by patient: Vincristine + Adriamycin + Dexamethasone
Adverse event in 53 year old female receiving Aredia (Pamidronate)
Reported by a physician from Japan on 2007-05-04
Patient: 53 year old female
Adverse reactions / side effects: Metastases TO Liver, Gingival Swelling, Osteomyelitis, Biopsy, Mucosal Inflammation, Gingival Pain, Osteonecrosis, Dental Treatment, Bone Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Zometa
Dosage: unk, unk
Indication: Metastases TO Bone
Start date: 2006-10-27
End date: 2006-12-22
Aredia
Dosage: 45 mg, unk
Indication: Metastases TO Bone
Start date: 2003-08-01
End date: 2006-10-14
Other drugs received by patient: Taxol
Adverse event in 53 year old female receiving Aredia (Pamidronate)
Reported by a physician from Japan on 2007-05-03
Patient: 53 year old female
Adverse reactions / side effects: Metastases TO Liver, Gingival Swelling, Osteomyelitis, Biopsy, Mucosal Inflammation, Gingival Pain, Osteonecrosis, Dental Treatment, Bone Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Zometa
Dosage: unk, unk
Indication: Metastases TO Bone
Start date: 2006-10-27
End date: 2006-12-22
Aredia
Dosage: 45 mg, unk
Indication: Metastases TO Bone
Start date: 2003-08-01
End date: 2006-10-14
Other drugs received by patient: Taxol
Adverse event in 84 year old male receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from France on 2007-04-18
Patient: 84 year old male
Adverse reactions / side effects: Osteonecrosis, Renal Failure, Tooth Extraction
Adverse event resulted in: disablity
Suspect drug(s):
Aredia
Dosage: 90 mg, qmo
Indication: Multiple Myeloma
Start date: 2001-03-01
End date: 2002-08-01
Zometa
Dosage: 4 mg, qmo
Indication: Multiple Myeloma
Start date: 2002-10-01
End date: 2004-12-01
Zometa
Dosage: 4 mg every 4 months
Other drugs received by patient: Melphalan; Melphalan; Prednisone TAB; Prednisone TAB
Adverse event in 69 year old female receiving Aredia (Pamidronate)
Reported by a individual with unspecified qualification from France on 2007-04-17
Patient: 69 year old female, weighing 87.0 kg (191.4 pounds)
Adverse reactions / side effects: Pseudarthrosis, Osteonecrosis, Pain, Pathological Fracture
Adverse event resulted in: disablity
Suspect drug(s):
Zometa
Dosage: unk, unk
Indication: Multiple Myeloma
Start date: 2003-05-16
End date: 2005-01-01
Aredia
Dosage: unk, unk
Indication: Multiple Myeloma
Start date: 2002-02-01
End date: 2003-05-15
Other drugs received by patient: Alkeran; Cortancyl
Adverse event in 69 year old female receiving Aredia (Pamidronate)
Reported by a physician from Cyprus on 2007-04-16
Patient: 69 year old female
Adverse reactions / side effects: Fistula, Osteonecrosis, Haemorrhage, Tooth Extraction, Osteomyelitis
Adverse event resulted in: disablity
Suspect drug(s):
Zometa
Dosage: 4 mg, qmo
Indication: Multiple Myeloma
Start date: 2001-07-31
End date: 2003-10-24
Zometa
Dosage: 4 mg, qmo
Start date: 2004-05-12
End date: 2004-11-01
Zometa
Dosage: 3 mg, qmo
Start date: 2004-12-20
End date: 2005-05-01
Aredia
Dosage: 90 mg, qmo
Indication: Multiple Myeloma
Start date: 2000-08-22
End date: 2001-07-03
Other drugs received by patient: Fluconazole; Penicillin; Septra; Zovirax; Thyroxin; Epoetin NOS; Vincristine + Adriamycin + Dexamethasone; Thalidomide; Dexamethasone
Adverse event in 69 year old male receiving Aredia (Pamidronate)
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-04-12
Patient: 69 year old male
Adverse reactions / side effects: Osteonecrosis, Dental Treatment, Tooth Extraction, Toothache, Infection
Adverse event resulted in: disablity
Suspect drug(s):
Aredia (Pamidronate)
Adverse event in 69 year old female receiving Aredia (Pamidronate)
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-04-05
Patient: 69 year old female
Adverse reactions / side effects: Osteonecrosis, Bone Lesion Excision
Adverse event resulted in: disablity
Suspect drug(s):
Aredia (Pamidronate)
Adverse event in male receiving Aredia (Pamidronate)
Reported by a lawyer from United States on 2007-03-29
Patient: male
Adverse reactions / side effects: Anxiety, Osteonecrosis, Pain, General Physical Health Deterioration, Decreased Interest
Adverse event resulted in: disablity
Suspect drug(s):
Aredia (Pamidronate)
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