Community-reported Actonel side effects:
Chronic Dry Eye, inflammation 2008-08-14 21:15:36
breast swelling 2008-09-28 14:11:25
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Total Actonel reports: 197.Actonel FDA safety alerts: 2007 2008 .
Reported deaths: 4 Reported hospitalizations: 67.
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FDA Reported Actonel Side Effects: osteonecrosis, arthralgia, bone pain, pain in jaw, pain in extremity, myalgia, jaw disorder, chest pain, nausea, condition aggravated, fall.
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Actonel Side Effects Report #5553367-5Physician from UNITED STATES reported ACTONEL problem on Aug 16, 2006. Male patient, 69 years of age, weighting 168.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: limb crushing injury, lower limb fracture, road traffic accident. ACTONEL dosage: unknown. During the same period patient was treated with VITAMIN E, SELENIUM, ACETYLSALICYLIC ACID SRT, GLUCOSAMINE W. Patient was hospitalized and became disabled. Patient recovered.
Actonel Side Effects Report #5553368-7
ACTONEL problem was reported by a Physician from UNITED STATES on Aug 09, 2007. Female patient, 48 years of age, weighting 179.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abscess jaw, bone disorder, fistula, infection, malnutrition, mouth ulceration, osteomyelitis, osteonecrosis, pain in jaw. ACTONEL dosage: 35 MG, WEEKLY, ORAL. During the same period patient was treated with FOSAMAX, EFFEXOR, ASPIRIN, COGENTIN, DITROPAN, LASIX, LEVOXYL, ADVAIR. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5553369-9
Physician from UNITED STATES reported ACTONEL problem on May 23, 2007. Female patient, 83 years of age, weighting 115.1 lb, was diagnosed with osteoporosis, arthralgia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abscess oral, bone erosion, excessive granulation tissue, oral candidiasis, osteonecrosis, osteosclerosis. ACTONEL dosage: unknown. During the same period patient was treated with PREDNISONE. Patient recovered.
Actonel Side Effects Report #5553370-5
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on May 03, 2007. Female patient, 75 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: rash pruritic, skin burning sensation. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient recovered.
Actonel Side Effects Report #5553371-7
Health Professional from UNITED STATES reported ACTONEL problem on Aug 07, 2007. Female patient, 75 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: lichen planus, osteomyelitis acute, osteonecrosis, primary sequestrum, tooth extraction. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with AMARYL, ICAPS, ASPIRIN, CALCIUM VIT D, TOPROL, LOTENSIN. Patient recovered.
Actonel Side Effects Report #5553372-9
ACTONEL problem was reported by a Physician from UNITED STATES on July 10, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: osteonecrosis, tooth extraction. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5553373-0
Health Professional from UNITED STATES reported ACTONEL problem on Sept 05, 2007. Female patient, 56 years of age, weighting 125.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: loose tooth, osteonecrosis, resorption bone increased, tooth extraction. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient recovered.
Actonel Side Effects Report #5553374-2
ACTONEL problem was reported by a Health Professional from UNITED STATES on Aug 09, 2007. Female patient, 52 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: crepitations, gingival pain, joint lock, mouth ulceration, oral intake reduced, oral pain, osteonecrosis, pain in jaw. ACTONEL dosage: unknown. During the same period patient was treated with FOSAMAX, KETOROLAC, GUAIFENESIN PSE, PLAQUENIL, ERYTHROMYCIN STEARATE, COLCHICUM JTL LIQ, POTASSIUM CHLORIDE, SEREVENT. Patient recovered.
Actonel Side Effects Report #5556747-7
Health Professional from UNITED STATES reported ACTONEL problem on Aug 09, 2007. Female patient, 71 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: jaw fracture, osteomyelitis, osteonecrosis, pain in jaw, subcutaneous abscess, swelling face. ACTONEL dosage: 35 MG, ONCE WEEKLY, ORAL. During the same period patient was treated with LEVOXYL, FUROSEMIDE, LACTULOSE, CALTRATE, ASPIRIN, HORSE CHESTNUT. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5556748-9
ACTONEL problem was reported by a Physician from UNITED STATES on Aug 09, 2007. Female patient was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, diarrhoea, exostosis, fracture malunion, glossitis, impaired healing, jaw cyst, jaw fracture, malnutrition. ACTONEL dosage: 30 MG, 1/WEEK, ORAL. During the same period patient was treated with FOSAMAX, PREDNISONE, METHOTREXATE, HYDROXYCHLOROQUINE SULPHATE, ESTRADIOL, PROPOXACET, RESTASIS. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5556749-0
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Aug 31, 2007. Female patient, 83 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: hip fracture. ACTONEL dosage: 35 MG ONCE A WEEK, ORAL. During the same period patient was treated with LOTREL, CALCIUM, VITAMIN D. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5556750-7
ACTONEL problem was reported by a Physician from UNITED STATES on Aug 15, 2007. Female patient, 43 years of age, was diagnosed with osteoporosis, multiple sclerosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: dental caries, dental necrosis, exostosis, gingivitis, headache, jaw disorder, lymph node pain, mastication disorder, oedema mouth. ACTONEL dosage: 35 MG ONCE A WEEK, ORAL. During the same period patient was treated with FOSAMAX, CORTICOSTEROIDS, VICODIN, DESIREL, LIPITOR, SINGULAIR, TEGRETOL, FLEXERIL. Patient recovered.
Actonel Side Effects Report #5556751-9
Physician from UNITED STATES reported ACTONEL problem on Aug 15, 2007. Female patient, 59 years of age, weighting 97.89 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone disorder, erythema, impaired healing, oral infection, osteomyelitis, osteonecrosis, resorption bone increased, swelling, tooth abscess. ACTONEL dosage: 35 MG, ONCE WEEKLY, ORAL. During the same period patient was treated with FOSAMAX, MOBIC, AMITRIPTYLINE, LIPITOR, BACTRIUM DS, PREMARIN, PREVACID, PLAVIX. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5556752-0
ACTONEL problem was reported by a Physician from UNITED STATES on Aug 15, 2007. Female patient was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abscess oral, anaemia of chronic disease, cellulitis, contusion, dental fistula, facial pain, hypoaesthesia, jaw disorder, osteomyelitis. ACTONEL dosage: 35 MG, ONCE WEEKLY. During the same period patient was treated with MELOXICAM, ATENOLOL, HYDROCORTISONE, WELLBUTRIN, ESTRADIOL, ACIPHEX, MOBIC, COZAAR. Patient recovered.
Actonel Side Effects Report #5556753-2
Physician from UNITED STATES reported ACTONEL problem on Sept 13, 2007. Female patient, 63 years of age, weighting 134.9 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia oral, oral infection, oral pain, osteomyelitis, osteonecrosis, purulent discharge, tooth extraction. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with FOSAMAX, LIPITOR, FLUOXETINE, COZAAR, GLYBURIDE, SINEMET. Patient recovered.
Actonel Side Effects Report #5556754-4
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 24, 2007. Female patient was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: fall, hip fracture, myalgia. ACTONEL dosage: 35 MG ONCE A WEEK, ORAL. During the same period patient was treated with ZETIA. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5556755-6
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Sept 25, 2007. Female patient, 73 years of age, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, back pain, bone pain, pain in jaw, tooth loss. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient recovered.
Actonel Side Effects Report #5556756-8
ACTONEL problem was reported by a Physician from UNITED STATES on Sept 25, 2007. Female patient, 66 years of age, was diagnosed with osteoporosis, rheumatoid arthritis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abscess jaw, aphthous stomatitis, bone disorder, cellulitis, erythema, facial pain, joint range of motion decreased, loose tooth, osteomyelitis. ACTONEL dosage: unknown. During the same period patient was treated with PREDNISONE, HYDROCHLOROTHIAZIDE, ASPIRIN, ASCORBIC ACID. Patient recovered.
Actonel Side Effects Report #5477715-X
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Oct 03, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthritis, fall, gastritis, refusal of treatment by patient. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5479332-4
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient, 54 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: carpal tunnel syndrome, chills, gait disturbance, hyperhidrosis, movement disorder, nausea, pain, pyrexia. ACTONEL dosage: 35 MG WEEKLY ORAL. Patient recovered.
Actonel Side Effects Report #5479333-6
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Oct 03, 2007. Female patient, 61 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: anaemia haemolytic autoimmune, blood immunoglobulin m abnormal, cold agglutinins positive, non-hodgkin's lymphoma, waldenstrom's macroglobulinaemia. ACTONEL dosage: 35 MG WEEKLY ORAL. Patient recovered.
Actonel Side Effects Report #5479334-8
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, back pain, discomfort, weight bearing difficulty. ACTONEL dosage: unknown. During the same period patient was treated with FOSAMAX. Patient recovered.
Actonel Side Effects Report #5480254-3
Physician from CANADA reported ACTONEL problem on Sept 26, 2007. Female patient, 81 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: hypertension, ovarian cancer. ACTONEL dosage: 35 MG, 1/WEEK, ORAL. During the same period patient was treated with SYNTHROID, MIACALCIN. Patient was hospitalized and became disabled. Patient recovered.
Actonel Side Effects Report #5480261-0
ACTONEL problem was reported by a Physician from AUSTRALIA on Sept 24, 2007. Female patient, 87 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: haematemesis, pneumonia. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with ENDONE, ARICEPT, OXAZEPAM. Patient died on 11/20/2006.
Actonel Side Effects Report #5480680-2
Physician from UNITED STATES reported ACTONEL problem on Sept 17, 2007. Female patient, 51 years of age, weighting 119.9 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, erythema, glomerulonephritis rapidly progressive, joint swelling, joint warmth, kidney enlargement, malaise, renal cortical necrosis, renal failure. ACTONEL dosage: 35 MG ONCE MONTHLY, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5483115-9
ACTONEL problem was reported by a Physician from UNITED STATES on Aug 27, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone disorder, chronic sinusitis, exostosis, hypoaesthesia oral, necrosis, oroantral fistula, osteonecrosis, pain in jaw, palatal disorder. ACTONEL dosage: unknown. During the same period patient was treated with FOSAMAX. Patient recovered.
Actonel Side Effects Report #5483171-8
Physician from FRANCE reported ACTONEL problem on Sept 28, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: impaired healing, osteitis, tooth abscess. ACTONEL dosage: 35 MG, 1/WEEK, ORAL. Patient recovered.
Actonel Side Effects Report #5483172-X
ACTONEL problem was reported by a Health Professional from FRANCE on Sept 27, 2007. Female patient, 93 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, dehydration, eating disorder, hypernatraemia, somnolence. ACTONEL dosage: unknown. During the same period patient was treated with OLMESARTAN MEDOXOMIL, RISPERDAL, KARDEGIC. Patient was hospitalized. Patient died on 08/02/2007.
Actonel Side Effects Report #5485939-0
Physician from JAPAN reported ACTONEL problem on Sept 28, 2007. Female patient, 89 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage. ACTONEL dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with ASPARA, VIT K CAP. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5487934-4
ACTONEL problem was reported by a Health Professional from UNITED STATES on Oct 12, 2007. Female patient, 59 years of age, weighting 171.0 lb, was diagnosed with postmenopause, prophylaxis, resorption bone increased and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal pain lower, abdominal pain upper, arthralgia, asthma, back pain, bladder pain, cough, dyspnoea. ACTONEL dosage: 35MG 1/WEEK PO. Patient recovered.
Actonel Side Effects Report #5488939-X
Physician from AUSTRALIA reported ACTONEL problem on Oct 05, 2007. Female patient, 61 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: breast cancer female. ACTONEL dosage: unknown. During the same period patient was treated with LIPITOR. Patient recovered.
Actonel Side Effects Report #5491338-8
ACTONEL problem was reported by a Physician from CANADA on Oct 05, 2007. Female patient, 81 years of age, weighting 95.02 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: hypertension, metastases to abdominal cavity, ovarian cancer metastatic. ACTONEL dosage: 35 MG, 1/WEEK, ORAL. During the same period patient was treated with SYNTHROID, MIACALCIN, PANTOPRAZOLE. Patient was hospitalized and became disabled. Patient recovered.
Actonel Side Effects Report #5493158-7
Health Professional from UNITED STATES reported ACTONEL problem on Oct 22, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, back disorder, bone disorder, mastication disorder, osteopenia, osteoporosis, pain in jaw, spinal disorder. ACTONEL dosage: 35 MG QWK ORAL. Patient recovered.
Actonel Side Effects Report #5493250-7
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 22, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: flatulence. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5494658-6
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Oct 23, 2007. Female patient, 50 years of age, weighting 108.0 lb, was diagnosed with bone density decreased and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, arthritis, immobile, joint stiffness, pain in extremity. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5500158-7
ACTONEL problem was reported by a Pharmacist from CANADA on Oct 10, 2007. Female patient, 59 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: brain neoplasm benign, convulsion, neoplasm progression. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with TOPAMAX, INDAPAMIDE, SIMVASTATIN, CALCIUM, VITAMIN D, CENTRUM SILVER. Patient recovered.
Actonel Side Effects Report #5503083-0
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Oct 16, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: lymphoma, thyroid cancer. ACTONEL dosage: 35 MG, ONCE WEEKLY, ORAL. During the same period patient was treated with NEURONTIN, INTERFERON, ATENOLOL, VAGIFEM, VITAMIN D, VITAMINS, CHLOR. Patient recovered.
Actonel Side Effects Report #5503600-0
ACTONEL problem was reported by a Physician from GERMANY on Oct 15, 2007. Female patient, 56 years of age, weighting 99.21 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: disease recurrence, diverticulitis. ACTONEL dosage: 35 MG, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5445959-9
Physician from AUSTRALIA reported ACTONEL problem on Aug 20, 2007. Female patient, 61 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: breast cancer female. ACTONEL dosage: unknown. During the same period patient was treated with LIPITOR. Patient recovered.
Actonel Side Effects Report #5447600-8
ACTONEL problem was reported by a Pharmacist from UNITED STATES on Sept 05, 2007. Male patient was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, arthralgia, myalgia. ACTONEL dosage: 75 MG TWO DAYS A MONTH PO. Patient recovered.
Actonel Side Effects Report #5450955-1
Health Professional from FRANCE reported ACTONEL problem on Aug 30, 2007. Female patient, 78 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abdominal pain lower, anaemia, asthenia, diabetes mellitus, hepatitis cholestatic, hepatomegaly, jaundice cholestatic, platelet count increased, scratch. ACTONEL dosage: 35 MG, 1/WEEK, ORAL. During the same period patient was treated with ELAVIL, TRILEPTAL, TERCIAN, PRAVASTATIN, AVLOCARDYL, ATARAX. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5451084-3
ACTONEL problem was reported by a Physician from CANADA on Aug 30, 2007. Female patient, 68 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: decreased appetite, eosinophilic pneumonia chronic, lung infiltration, night sweats. ACTONEL dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with CALCIUM CARBONATE, VITAMIN D. Patient was hospitalized and became disabled. Patient recovered.
Actonel Side Effects Report #5451085-5
Health Professional from UNITED KINGDOM reported ACTONEL problem on Aug 30, 2007. Female patient, 81 years of age, weighting 103.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: barrett's oesophagus, dysphagia, oesophagitis, regurgitation. ACTONEL dosage: 5 MG, DAILY, ORAL. During the same period patient was treated with ALENDRONATE, ADCAL, ASPIRIN, DOCUSATE, IPRATROPIUM BROMIDE, LACTULOSE, SENNA, TRIFLUOPERAZINE. Patient was hospitalized. Patient died on 06/15/2007.
Actonel Side Effects Report #5452764-6
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 21, 2007. Female patient was diagnosed with systemic lupus erythematosus and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: alopecia, condition aggravated, oral disorder, sjogren's syndrome. ACTONEL dosage: unknown. During the same period patient was treated with ROZEREM, CELLCEPT, PLAQUENIL. Patient recovered.
Actonel Side Effects Report #5455730-X
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Aug 31, 2007. Female patient, 83 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: diverticulitis, synovial cyst. ACTONEL dosage: 35 MG ONCE A WEEK, ORAL. During the same period patient was treated with LOTREL, CALCIUM, VITAMIN D. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5456934-2
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 17, 2007. Female patient, weighting 120.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: eye infection, uveitis. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5458143-X
Pharmacist from FRANCE reported ACTONEL problem on Sept 04, 2007. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, eating disorder, fatigue, gamma-glutamyltransferase increased, hyperbilirubinaemia, nausea, ocular icterus, urine abnormality. ACTONEL dosage: 35 MG, 1/WEEK, ORAL. During the same period patient was treated with FENOFIBRATE, MICARDIS, GINKORT, SPASFON, DAFALFAN, PROTELOS. Patient recovered.
Actonel Side Effects Report #5466363-3
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 07, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: failure of implant, gingival infection, loose tooth, resorption bone increased, tooth extraction. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with VITAMINS. Patient recovered.
Actonel Side Effects Report #5466364-5
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Sept 11, 2007. Female patient, 54 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: pelvic neoplasm. ACTONEL dosage: unknown. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5467094-6
ACTONEL problem was reported by a Physician from SLOVAKIA (Slovak Republic) on Sept 07, 2007. Female patient was diagnosed with osteoporosis postmenopausal and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: extraocular muscle disorder, eye disorder, eye luxation, eye oedema, eyelid ptosis, lacrimation increased. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5467103-4
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Sept 21, 2007. Female patient, 54 years of age, weighting 125.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, arthritis, arthropathy, asthenia, bone pain, burning sensation, gait disturbance, joint swelling. ACTONEL dosage: 35 MG EACH WEEK PO. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5468147-9
ACTONEL problem was reported by a Health Professional from NORWAY on Sept 12, 2007. Male patient, 65 years of age, was diagnosed with prostate cancer and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: nephrolithiasis, pain. ACTONEL dosage: 30 MG, DAILY, ORAL. During the same period patient was treated with DOCETAXEL, PREDNISON. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5468152-2
Pharmacist from UNITED KINGDOM reported ACTONEL problem on Sept 13, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abortion spontaneous. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5470541-7
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 27, 2007. Female patient, 58 years of age, weighting 133.0 lb, was diagnosed with osteopenia, osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, headache, hypoventilation, jaw disorder, muscle strain, musculoskeletal pain, musculoskeletal stiffness, neck pain. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5406726-5
Health Professional from UNITED KINGDOM reported ACTONEL problem on July 26, 2007. Female patient, 80 years of age, was diagnosed with arthritis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: crying, gait disturbance, impaired driving ability, muscle spasms, myalgia, pain in extremity. ACTONEL dosage: 35MG, 1/WEEK, ORAL. During the same period patient was treated with PREDNISOLONE, GLUCOSAMINE, LANSOPRAZOLE, NAPROXEN, LEVOTHYROXINE. Patient recovered.
Actonel Side Effects Report #5409358-8
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 07, 2007. Female patient, weighting 140.0 lb, was diagnosed with bone disorder and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone pain, musculoskeletal pain, musculoskeletal stiffness, myalgia, no therapeutic response. ACTONEL dosage: 35MG WEEKLY PO. Patient recovered.
Actonel Side Effects Report #5409369-2
Consumer or non-health professional from HONG KONG reported ACTONEL problem on Aug 01, 2007. Female patient, 70 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone pain, chest pain, heart rate abnormal, nausea. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5409371-0
ACTONEL problem was reported by a Consumer or non-health professional from AUSTRALIA on July 25, 2007. Female patient, 71 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, renal failure. ACTONEL dosage: 35 MG, ORAL. During the same period patient was treated with AVAPRO HCT, TAZAC. Patient recovered.
Actonel Side Effects Report #5409437-5
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Aug 08, 2007. Female patient, 55 years of age, weighting 120.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, bone pain, condition aggravated, osteopenia, osteoporosis. ACTONEL dosage: 35 MG ONCE A WEEK PO. Patient recovered.
Actonel Side Effects Report #5409475-2
ACTONEL problem was reported by a Physician from UNITED STATES on Aug 07, 2007. Female patient, weighting 130.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: osteonecrosis. ACTONEL dosage: 35MG ONCE/WEEK PO. During the same period patient was treated with BONIVA. Patient recovered.
Actonel Side Effects Report #5411756-3
Physician from GERMANY reported ACTONEL problem on Aug 03, 2007. Female patient, 62 years of age, was diagnosed with osteoporosis, hypertension, breast cancer and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: retinal vascular disorder, vision blurred, visual disturbance. ACTONEL dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, FEMARA. Patient recovered.
Actonel Side Effects Report #5416482-2
ACTONEL problem was reported by a Physician from AUSTRALIA on Aug 01, 2007. Female patient, 63 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: gastrooesophageal reflux disease, non-cardiac chest pain, oesophagitis. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with AROPAX, ATACAND, KLACID. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5419613-3
Physician from UNITED STATES reported ACTONEL problem on Aug 16, 2007. Female patient, 80 years of age, weighting 111.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: osteonecrosis. ACTONEL dosage: 35 MG WEEKLY PO. Patient recovered.
Actonel Side Effects Report #5420848-4
ACTONEL problem was reported by a Physician from CANADA on Aug 08, 2007. Female patient was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: pneumonitis. ACTONEL dosage: 35 MG, 1/WEEK, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5421736-X
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on Aug 06, 2007. Female patient, 79 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: alopecia, anaemia, myocardial infarction, pain in jaw. ACTONEL dosage: 35 MG, 1/WEEK, ORAL; 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with ZOCOR, LEXAPRO, SINGULAIR, VITAMIN B12, KETOPROFEN, HORMONES AND RELATED AGENTS. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5422318-6
ACTONEL problem was reported by a Physician from JAPAN on Aug 10, 2007. Female patient, 63 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: decreased appetite. ACTONEL dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with HALCION. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5422319-8
Consumer or non-health professional from CANADA reported ACTONEL problem on Aug 10, 2007. Female patient, 81 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: hypertension, ovarian cancer. ACTONEL dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with SYNTHROID, MIACALCIN. Patient recovered.
Actonel Side Effects Report #5429277-0
ACTONEL problem was reported by a Physician from CANADA on Aug 21, 2007. Female patient, 78 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: decreased appetite, eosinophilic pneumonia chronic, night sweats. ACTONEL dosage: 35 MG, 1 /WEEK, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5429286-1
Physician from SWITZERLAND reported ACTONEL problem on Aug 16, 2007. Female patient, weighting 7.94 lb, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: kidney enlargement, neonatal disorder. ACTONEL dosage: unknown. During the same period patient was treated with IMUREK, PREDNISONE, PAROXETINE. Patient recovered.
Actonel Side Effects Report #5385221-6
ACTONEL problem was reported by a Consumer or non-health professional from AUSTRALIA on June 28, 2007. Male patient, 45 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: haematemesis, pain. ACTONEL dosage: 5MG DAILY, ORAL. Patient recovered.
Actonel Side Effects Report #5385223-X
Physician from LITHUANIA reported ACTONEL problem on June 27, 2007. Female patient, 70 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone marrow oedema, groin pain, neoplasm, osteonecrosis. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient recovered.
Actonel Side Effects Report #5387090-7
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on June 29, 2007. Male patient, 86 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: fall, hypotension, loss of consciousness, presyncope. ACTONEL dosage: 35 MG WEEKLY, ORAL. During the same period patient was treated with DIOVAN, BETAPACE, LUPRON, CADUET, POSTURE D, FOLIC ACID, LUTEIN, COUMADIN. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5387208-6
Physician from CANADA reported ACTONEL problem on June 29, 2007. Female patient, 64 years of age, weighting 122.4 lb, was diagnosed with osteoporosis prophylaxis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage. ACTONEL dosage: 35 MG, 1 /WEEK, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5389586-0
ACTONEL problem was reported by a Consumer or non-health professional from HONG KONG on June 28, 2007. Female patient, 70 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone pain, chest pain, heart rate abnormal, hyperthyroidism, nausea. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5389893-1
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 16, 2007. Female patient, weighting 150.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: muscular weakness, paralysis. ACTONEL dosage: 35 MG 1X MOUTH. Patient was hospitalized and became disabled. Patient recovered.
Actonel Side Effects Report #5389936-5
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on July 17, 2007. Female patient, 55 years of age, weighting 151.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: dry eye, eye haemorrhage, eye irritation, eye movement disorder, eye pain, eye swelling, headache, photophobia, visual disturbance. ACTONEL dosage: 35 MG -1 TABLET ORALLY WEEKLY - ORALLY ONCE A WEEK PO. Patient recovered.
Actonel Side Effects Report #5391259-5
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 05, 2007. Female patient, 68 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, gait disturbance, joint range of motion decreased, osteoarthritis. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with DYNACIRC CR, SPIRONOLACTONE, SYNTHROID, CALCIUM, GLUCOSAMINE, CRANBERRY. Patient recovered.
Actonel Side Effects Report #5393056-3
ACTONEL problem was reported by a Consumer or non-health professional from AUSTRALIA on July 09, 2007. Female patient, 76 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: blood calcium increased, dysphagia, parapharyngeal abscess. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5398822-6
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 25, 2007. Female patient, weighting 125.0 lb, was diagnosed with heart rate irregular and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: cardiac valve disease, heart rate irregular. ACTONEL dosage: 35 MG 1 WEEK. Patient recovered.
Actonel Side Effects Report #5400135-0
ACTONEL problem was reported by a Consumer or non-health professional from CANADA on July 11, 2007. Female patient, 80 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, blood pressure increased, corneal deposits, corneal disorder, eye inflammation, eye pain, nervousness. ACTONEL dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with CALCIUM WITH VITAMIN D, TRIMETHOPRIM, ASADOL. Patient recovered.
Actonel Side Effects Report #5400141-6
Physician from GERMANY reported ACTONEL problem on July 13, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, hypotension, nausea, vomiting. ACTONEL dosage: 35 MG, 1 ONLY, ORAL. During the same period patient was treated with HORMONE ANTAGONISTS AND RELATED AGENTS. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5400553-0
ACTONEL problem was reported by a Physician from AUSTRALIA on July 09, 2007. Female patient, 57 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: osteonecrosis, thyroid cancer. ACTONEL dosage: unknown. During the same period patient was treated with PANTOPRAZOLE. Patient recovered.
Actonel Side Effects Report #5402402-3
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 30, 2007. Female patient, 65 years of age, weighting 116.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain upper, flatulence, lethargy, nausea. ACTONEL dosage: unknown. Patient recovered.
Actonel Side Effects Report #5385221-6
ACTONEL problem was reported by a Consumer or non-health professional from AUSTRALIA on June 28, 2007. Male patient, 45 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: haematemesis, pain. ACTONEL dosage: 5MG DAILY, ORAL. Patient recovered.
Actonel Side Effects Report #5385223-X
Physician from LITHUANIA reported ACTONEL problem on June 27, 2007. Female patient, 70 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone marrow oedema, groin pain, neoplasm, osteonecrosis. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient recovered.
Actonel Side Effects Report #5387090-7
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on June 29, 2007. Male patient, 86 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: fall, hypotension, loss of consciousness, presyncope. ACTONEL dosage: 35 MG WEEKLY, ORAL. During the same period patient was treated with DIOVAN, BETAPACE, LUPRON, CADUET, POSTURE D, FOLIC ACID, LUTEIN, COUMADIN. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5387208-6
Physician from CANADA reported ACTONEL problem on June 29, 2007. Female patient, 64 years of age, weighting 122.4 lb, was diagnosed with osteoporosis prophylaxis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage. ACTONEL dosage: 35 MG, 1 /WEEK, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5389586-0
ACTONEL problem was reported by a Consumer or non-health professional from HONG KONG on June 28, 2007. Female patient, 70 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: bone pain, chest pain, heart rate abnormal, hyperthyroidism, nausea. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5389893-1
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 16, 2007. Female patient, weighting 150.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: muscular weakness, paralysis. ACTONEL dosage: 35 MG 1X MOUTH. Patient was hospitalized and became disabled. Patient recovered.
Actonel Side Effects Report #5389936-5
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on July 17, 2007. Female patient, 55 years of age, weighting 151.0 lb, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: dry eye, eye haemorrhage, eye irritation, eye movement disorder, eye pain, eye swelling, headache, photophobia, visual disturbance. ACTONEL dosage: 35 MG -1 TABLET ORALLY WEEKLY - ORALLY ONCE A WEEK PO. Patient recovered.
Actonel Side Effects Report #5391259-5
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 05, 2007. Female patient, 68 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, gait disturbance, joint range of motion decreased, osteoarthritis. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with DYNACIRC CR, SPIRONOLACTONE, SYNTHROID, CALCIUM, GLUCOSAMINE, CRANBERRY. Patient recovered.
Actonel Side Effects Report #5393056-3
ACTONEL problem was reported by a Consumer or non-health professional from AUSTRALIA on July 09, 2007. Female patient, 76 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: blood calcium increased, dysphagia, parapharyngeal abscess. ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5398822-6
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 25, 2007. Female patient, weighting 125.0 lb, was diagnosed with heart rate irregular and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: cardiac valve disease, heart rate irregular. ACTONEL dosage: 35 MG 1 WEEK. Patient recovered.
Actonel Side Effects Report #5400135-0
ACTONEL problem was reported by a Consumer or non-health professional from CANADA on July 11, 2007. Female patient, 80 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, blood pressure increased, corneal deposits, corneal disorder, eye inflammation, eye pain, nervousness. ACTONEL dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with CALCIUM WITH VITAMIN D, TRIMETHOPRIM, ASADOL. Patient recovered.
Actonel Side Effects Report #5400141-6
Physician from GERMANY reported ACTONEL problem on July 13, 2007. Female patient was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, hypotension, nausea, vomiting. ACTONEL dosage: 35 MG, 1 ONLY, ORAL. During the same period patient was treated with HORMONE ANTAGONISTS AND RELATED AGENTS. Patient was hospitalized. Patient recovered.
Actonel Side Effects Report #5400553-0
ACTONEL problem was reported by a Physician from AUSTRALIA on July 09, 2007. Female patient, 57 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: osteonecrosis, thyroid cancer. ACTONEL dosage: unknown. During the same period patient was treated with PANTOPRAZOLE. Patient recovered.
Actonel Side Effects Report #5402402-3
Consumer or non-health professional from UNITED STATES reported ACTONEL problem on July 30, 2007. Female patient, 65 years of age, weighting 116.0 lb, was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain upper, flatulence, lethargy, nausea. ACTONEL dosage: unknown. Patient recovered.
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