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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Actonel (Risedronate). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (179)
Cases resulting in a serious event (167)
Cases resulting in death (9)
Cases resulting in life threatening events (8)
Cases resulting in hospitalization (74)
Cases resulting in disability (32)
Cases resulting in other serious reactions (99)
Below is a sample of reports where side effects / adverse reactions may be related to Actonel (Risedronate). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 61 year old female receiving Actonel (Risedronate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31
Patient: 61 year old female, weighing 61.0 kg (134.2 pounds)
Adverse reactions / side effects: Wrist Fracture, Upper Limb Fracture, Osteomyelitis, Chronic Obstructive Pulmonary Disease, Anxiety, Carotid Artery Stenosis, HIP Fracture, Renal Failure, Osteonecrosis, Alcoholism, Diarrhoea, Upper Gastrointestinal Haemorrhage, Depression, Bronchitis, Tendonitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Fosamax
Administration route: Oral
Indication: Osteoporosis
Start date: 2003-01-27
End date: 2005-01-24
Fosamax
Administration route: Oral
Indication: Osteopenia
Start date: 2003-01-27
End date: 2005-01-24
Actonel
Administration route: Oral
Indication: Osteoporosis
Start date: 2005-01-24
End date: 2005-05-01
Adverse event in female receiving Actonel (Risedronate)
Reported by a individual with unspecified qualification from United States on 2007-10-29
Patient: female
Adverse reactions / side effects: Thyroid Cancer, Lymphoma
Suspect drug(s):
Actonel (Risedronate)
Other drugs received by patient: Neurontin; Interferon (Interferon); Atenolol; Vagifem; Vitamin D; Vitamins; Chlor-Trimeton
Adverse event in 56 year old female receiving Actonel (Risedronate)
Reported by a physician from Germany on 2007-10-29
Patient: 56 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Disease Recurrence, Diverticulitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Actonel (Risedronate)
Adverse event in female receiving Actonel (Risedronate)
Reported by a physician from Japan on 2007-10-26
Patient: female, weighing 67.0 kg (147.4 pounds)
Adverse reactions / side effects: Tuberculosis, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Indication: Rheumatoid Arthritis
Mobic
Administration route: Oral
Indication: Rheumatoid Arthritis
Bredinin
Administration route: Oral
Indication: Rheumatoid Arthritis
Rimatil
Administration route: Oral
Indication: Rheumatoid Arthritis
Actonel
Administration route: Oral
Indication: Osteoporosis
Lansoprazole
Administration route: Oral
Indication: Reflux Oesophagitis
Cytotec
Dosage: 600rg
Administration route: Oral
Indication: Gastritis
Rheumatrex
Administration route: Oral
Indication: Rheumatoid Arthritis
Other drugs received by patient: Isoniazid
Adverse event in 60 year old female receiving Actonel (Risedronate)
Reported by a physician from United States on 2007-10-26
Patient: 60 year old female
Adverse reactions / side effects: Pleuritic Pain, Tooth Abscess, Fear, Pyrexia, Fall, Renal Artery Stenosis, Weight Increased, Vascular Pseudoaneurysm, Intervertebral Disc Degeneration, Depression, Carpal Tunnel Syndrome, Vomiting, Monoplegia, Dysphagia, Spondylolisthesis, Renal Cyst, Nephrosclerosis, Anxiety, Osteonecrosis, Limb Injury, Back Injury, Infection
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Fosamax
Administration route: Oral
Start date: 2001-09-20
End date: 2003-11-15
Fosamax
Administration route: Oral
Start date: 2000-01-01
Actonel
Start date: 2003-12-23
End date: 2005-04-07
Other drugs received by patient: Lasix; Lasix; Lipitor; Lipitor; Librax; Tigan; Plendil; Vitamins (Unspecified); Potassium (Unspecified); Vitamin B Complex; Calcium (Unspecified); Advil; Atenolol; Zocor; Xanax; [therapy Unspecified]
Adverse event in 59 year old female receiving Actonel (Risedronate)
Reported by a pharmacist from Canada on 2007-10-25
Patient: 59 year old female
Adverse reactions / side effects: Brain Neoplasm Benign, Neoplasm Progression, Convulsion
Suspect drug(s):
Actonel (Risedronate)
Other drugs received by patient: Topamax; Indapamide; Simvastatin; Calcium (Calcium); Vitamin D / 00107901 / (Ergocalciferol); Centrum Silver / 01292501 / (Zinc, Vitamins Nos, Vitamin B Nos, Tocopher
Adverse event in 61 year old female receiving Actonel (Risedronate)
Reported by a consumer/non-health professional from Spain on 2007-10-24
Patient: 61 year old female
Adverse reactions / side effects: Drug Interaction, Spontaneous Haematoma
Suspect drug(s):
Amoxicillin and Clavulanate Potassium
Dosage: 1500mg per day
Administration route: Oral
Indication: Tooth Abscess
Start date: 2007-09-03
End date: 2007-09-10
Iscover
Dosage: 75mg per day
Administration route: Oral
Indication: Cerebral Venous Thrombosis
Start date: 2001-01-01
Ideos
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Actonel
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 50 year old female receiving Actonel (Risedronate)
Reported by a consumer/non-health professional from United States on 2007-10-23
Patient: 50 year old female, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Pain in Extremity, Arthralgia, Arthritis, Immobile, Joint Stiffness
Suspect drug(s):
Actonel (Risedronate)
Adverse event in 55 year old female receiving Actonel (Risedronate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-22
Patient: 55 year old female, weighing 71.0 kg (156.2 pounds)
Adverse reactions / side effects: HIP Fracture, Osteonecrosis, Fracture, Ear Infection, Osteomyelitis, Depression, Oroantral Fistula, Ankle Fracture
Adverse event resulted in: hospitalization
Suspect drug(s):
Fosamax
Administration route: Oral
Indication: Bone Density Decreased
Start date: 1998-11-01
Fosamax
Administration route: Oral
End date: 2001-12-01
Actonel
Administration route: Oral
Indication: Bone Density Decreased
Start date: 2001-12-01
Actonel
Administration route: Oral
End date: 2004-09-01
Adverse event in female receiving Actonel (Risedronate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-22
Patient: female
Adverse reactions / side effects: Osteoporosis, Osteopenia, Arthralgia, Mastication Disorder, Bone Disorder, Spinal Disorder, Pain in JAW, Back Disorder
Suspect drug(s):
Actonel (Risedronate)
Adverse event in female receiving Actonel (Risedronate)
Reported by a individual with unspecified qualification from United States on 2007-10-22
Patient: female
Adverse reactions / side effects: Flatulence
Suspect drug(s):
Actonel (Risedronate)
Adverse event in 81 year old female receiving Actonel (Risedronate)
Reported by a physician from Canada on 2007-10-17
Patient: 81 year old female, weighing 43.1 kg (94.8 pounds)
Adverse reactions / side effects: Ovarian Cancer Metastatic, Metastases TO Abdominal Cavity, Hypertension
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Actonel (Risedronate)
Other drugs received by patient: Synthroid; Miacalcin; Pantoprazole Sodium
Adverse event in 61 year old female receiving Actonel (Risedronate)
Reported by a physician from Australia on 2007-10-16
Patient: 61 year old female
Adverse reactions / side effects: Breast Cancer Female
Suspect drug(s):
Actonel (Risedronate)
Other drugs received by patient: Lipitor
Adverse event in 59 year old female receiving Actonel (Risedronate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-12
Patient: 59 year old female, weighing 77.6 kg (170.6 pounds)
Adverse reactions / side effects: Asthma, Abdominal Pain, Abdominal Pain Lower, Back Pain, Movement Disorder, Dyspnoea, Pain in Extremity, Pain, Bladder Pain, Musculoskeletal Chest Pain, Abdominal Pain Upper, Arthralgia, Flank Pain, Gait Disturbance, Gastrooesophageal Reflux Disease, Cough, Influenza Like Illness
Suspect drug(s):
Actonel
Dosage: 35mg 1/week po
Administration route: Oral
Indication: Postmenopause
Start date: 2007-10-01
End date: 2007-10-01
Actonel
Dosage: 35mg 1/week po
Administration route: Oral
Indication: Prophylaxis
Start date: 2007-10-01
End date: 2007-10-01
Actonel
Dosage: 35mg 1/week po
Administration route: Oral
Indication: Resorption Bone Increased
Start date: 2007-10-01
End date: 2007-10-01
Adverse event in 89 year old female receiving Actonel (Risedronate)
Reported by a physician from Japan on 2007-10-12
Patient: 89 year old female
Adverse reactions / side effects: Gastrointestinal Haemorrhage
Adverse event resulted in: hospitalization
Suspect drug(s):
Actonel (Risedronate)
Other drugs received by patient: Aspara-CA (Aspartate Calcium); VIT K CAP
Adverse event in female receiving Actonel (Risedronate)
Reported by a physician from Japan on 2007-10-10
Patient: female, weighing 47.0 kg (103.4 pounds)
Adverse reactions / side effects: Pneumocystis Jiroveci Pneumonia, Headache
Adverse event resulted in: hospitalization
Suspect drug(s):
Remicade
Remicade
Indication: Rheumatoid Arthritis
Pravastatin
Administration route: Oral
Indication: Hyperlipidaemia
Rheumatrex
Administration route: Oral
Indication: Rheumatoid Arthritis
Orgadrone
Indication: Rheumatoid Arthritis
Predonine
Administration route: Oral
Indication: Rheumatoid Arthritis
Actonel
Administration route: Oral
Indication: Osteoporosis
Other drugs received by patient: Decadron
Adverse event in female receiving Actonel (Risedronate)
Reported by a physician from United States on 2007-10-09
Patient: female
Adverse reactions / side effects: Tooth Loss, Wound Dehiscence, Necrosis, Periodontal Disease, Tooth Extraction, Oroantral Fistula, Palatal Disorder, Hypoaesthesia Oral, Osteonecrosis, Chronic Sinusitis, Bone Disorder, Exostosis, Pain in JAW
Suspect drug(s):
Actonel
Dosage: oral
Administration route: Oral
Start date: 2002-01-01
End date: 2006-05-01
Fosamax
Adverse event in female receiving Actonel (Risedronate)
Reported by a physician from France on 2007-10-09
Patient: female
Adverse reactions / side effects: Tooth Abscess, Impaired Healing, Osteitis
Suspect drug(s):
Actonel (Risedronate)
Adverse event in 93 year old female receiving Actonel (Risedronate)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-09
Patient: 93 year old female
Adverse reactions / side effects: Blood Urea Increased, Dehydration, General Physical Health Deterioration, Hypernatraemia, Blood Creatine Increased, Somnolence, Eating Disorder
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Actonel
Dosage: oral
Administration route: Oral
Start date: 2004-01-01
End date: 2007-07-21
Olmesartan Medoxomil
Dosage: oral
Administration route: Oral
End date: 2007-07-12
Risperdal
Dosage: 2 mg, daily, oral
Administration route: Oral
Start date: 2004-01-01
End date: 2007-07-21
Kardegic / 00002703 / (Acetylsalicylate Lysine)
Dosage: oral
Administration route: Oral
End date: 2007-07-21
Adverse event in 55 year old female receiving Actonel (Risedronate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-05
Patient: 55 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Bone Pain, Lower Limb Fracture, Fall, Arrhythmia, Osteonecrosis, Arthralgia, Gastrointestinal Disorder, Bone Disorder, Eye Disorder, Coccydynia
Suspect drug(s):
Fosamax
Actonel
Adverse event in female receiving Actonel (Risedronate)
Reported by a individual with unspecified qualification from United States on 2007-10-03
Patient: female
Adverse reactions / side effects: Refusal of Treatment by Patient, Fall, Arthritis, Gastritis
Suspect drug(s):
Actonel (Risedronate)
Adverse event in female receiving Actonel (Risedronate)
Reported by a individual with unspecified qualification from United States on 2007-10-03
Patient: female
Adverse reactions / side effects: Back Pain, Weight Bearing Difficulty, Arthralgia, Discomfort
Suspect drug(s):
Actonel
Dosage: oral
Administration route: Oral
Fosamax
Dosage: oral
Administration route: Oral
Adverse event in 51 year old female receiving Actonel (Risedronate)
Reported by a physician from United States on 2007-10-03
Patient: 51 year old female, weighing 54.4 kg (119.7 pounds)
Adverse reactions / side effects: Renal Cortical Necrosis, Kidney Enlargement, Glomerulonephritis Rapidly Progressive, Erythema, Renal Failure, Malaise, Joint Swelling, Arthralgia, Joint Warmth
Adverse event resulted in: hospitalization
Suspect drug(s):
Actonel (Risedronate)
Adverse event in female receiving Actonel (Risedronate)
Reported by a individual with unspecified qualification from United States on 2007-10-03
Patient: female
Adverse reactions / side effects: Pain, Lethargy
Suspect drug(s):
Fosamax
Dosage: oral
Administration route: Oral
Actonel
Dosage: oral
Administration route: Oral
Adverse event in receiving Actonel (Risedronate)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-03
Patient:
Adverse reactions / side effects: Bone Pain, Fatigue, Chest Pain, Blood Cholesterol Increased, Nasal Dryness, Muscle Spasms, Ilium Fracture, Pain in Extremity, Hypoaesthesia, Vocal Cord Disorder, Paraesthesia, Gastrointestinal Pain, Arthralgia, Joint Swelling, Dysphonia, Vision Blurred, Influenza Like Illness
Suspect drug(s):
Fosamax
Start date: 2006-01-01
End date: 2006-05-01
Actonel
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