ACTINOMYCOSIS side effect
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Drugs associated with ACTINOMYCOSIS
ALBUREX AREDIA AZATHIOPRINE BONDRONAT COPPER CYCLOPHOSPHAMIDE DOXYCYCLINE FEMARA FERROUS FOSAMAX HERCEPTIN IBANDRONIC IMMUNOGLOBULINS JANUVIA MIRENA PAMIDRONATE PARAGARD PEPCID PREDNISOLONE PREDNISONE THALOMID TRICOR ZOLEDRONATE ZOLEDRONIC ZOMETAAredia Side Effects Report #5648449-3
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Feb 25, 2008. Female patient, 69 years of age, weighting 129.2 lb, was diagnosed with breast cancer, metastases to bone and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone debridement, bone disorder, bone operation, breath odour, chronic sinusitis, computerised tomogram abnormal, dental caries, dental discomfort, . AREDIA dosage: 90MG IV Q3 WEEKS. During the same period patient was treated with ZOMETA, PRILOSEC, FEMARA, VALIUM, AROMASIN, XELODA. Patient recovered.
Aredia Side Effects Report #5648515-2
AREDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, 67 years of age, weighting 167.0 lb, was diagnosed with metastases to bone, breast cancer and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anxiety, bone disorder, bone operation, breath odour, cataract operation, debridement, dental operation, erythema, . AREDIA dosage: 90 MG MONTHLY. During the same period patient was treated with ZOMETA, FOSAMAX, HERCEPTIN, NAVELBINE, TAXOL, LIPITOR, ARANESP. Patient recovered.
Azathioprine Side Effects Report #5661187-6
Consumer or non-health professional from TURKEY reported AZATHIOPRINE problem on Feb 19, 2008. Female patient, 55 years of age, was diagnosed with crohn's disease and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: actinomycosis, iucd complication, necrosis, pelvic abscess, uterine rupture, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with CORTICOSTEROIDS. Patient was hospitalized. Patient recovered.
Prednisone Side Effects Report #5669990-3
PREDNISONE problem was reported by a Consumer or non-health professional from on Mar 12, 2008. Male patient, 47 years of age, was diagnosed with systemic lupus erythematosus, histoplasmosis, actinomycosis and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: actinomycosis, histoplasmosis, tongue necrosis, . PREDNISONE dosage: unknown. During the same period patient was treated with CIPROFLOXACIN, AMPHOTERICIN B, PENICILLIN. Patient was hospitalized. Patient recovered.
Ibandronic Side Effects Report #5671181-7
Health Professional from UNITED KINGDOM reported IBANDRONIC ACID problem on Mar 03, 2008. Female patient, 51 years of age, was diagnosed with breast cancer and was treated with IBANDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, breath odour, dental caries, facial pain, jaw disorder, mouth ulceration, mucosal inflammation, . IBANDRONIC ACID dosage: unknown. During the same period patient was treated with CLODRONATE DI, ARIMIDEX, AROMASIN, CYCLOPHOSPHAMIDE, FLUOROURACIL, METHOTREXATE, TAMOXIFEN, ZOLEDRONIC ACID. Patient recovered.
Ibandronic Side Effects Report #5673100-6
IBANDRONIC ACID problem was reported by a Health Professional from UNITED KINGDOM on Mar 04, 2008. Female patient, 51 years of age, was treated with IBANDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, breath odour, dental caries, facial pain, jaw disorder, mouth ulceration, mucosal inflammation, nasal disorder, . IBANDRONIC ACID dosage: unknown. During the same period patient was treated with ZOLEDRONIC ACID, CLODRONATE DI. Patient recovered.
Ibandronic Side Effects Report #5675721-3
Health Professional from UNITED KINGDOM reported IBANDRONIC ACID problem on Mar 10, 2008. Female patient, 51 years of age, was diagnosed with breast cancer and was treated with IBANDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, breath odour, dental caries, facial pain, jaw disorder, mouth ulceration, mucosal inflammation, . IBANDRONIC ACID dosage: unknown. During the same period patient was treated with CLODRONATE DI, ARIMIDEX, AROMASIN, CYCLOPHOSPHAMIDE, FLUOROURACIL, METHOTREXATE, TAMOXIFEN CITRATE, ZOLEDRONIC ACID. Patient recovered.
Azathioprine Side Effects Report #5680814-0
AZATHIOPRINE problem was reported by a Consumer or non-health professional from on Mar 24, 2008. Female patient, 55 years of age, was diagnosed with crohn's disease, actinomycosis and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: actinomycosis, uterine rupture, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with STEROIDS, PENICILLIN G. Patient recovered.
Mirena Side Effects Report #5685679-9
Consumer or non-health professional from UNITED STATES reported MIRENA problem on Sept 04, 2007. Female patient, 27 years of age, weighting 136.7 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, metrorrhagia, . MIRENA dosage: unknown. Patient recovered.
Zometa Side Effects Report #5615011-8
ZOMETA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2008. Male patient, 73 years of age, weighting 160.0 lb, was diagnosed with breast cancer metastatic, aortic valve incompetence, blood cholesterol and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, alpha haemolytic streptococcal infection, anxiety, aortic valve stenosis, debridement, inflammation, injury, oesophageal ulcer, oesophagitis, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA, PROCARDIA, ZOCOR. Patient recovered.
Fosamax Side Effects Report #5616207-1
Physician from UNITED STATES reported FOSAMAX problem on Jan 28, 2008. Female patient, 74 years of age, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinomycosis, adverse event, anxiety, fistula, oedema peripheral, osteomyelitis, osteonecrosis, postmenopausal haemorrhage, transient ischaemic attack, . FOSAMAX dosage: unknown. During the same period patient was treated with THALIDOMIDE. Patient was hospitalized and became disabled. Patient recovered.
Tricor Side Effects Report #5624157-X
TRICOR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2008. Female patient, 74 years of age, was diagnosed with metastases to bone, pain, prophylaxis, osteoporosis, sinus congestion and was treated with TRICOR. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anxiety, blood creatinine increased, bone debridement, bone disorder, crepitations, dental caries, endodontic procedure, gingivitis, . TRICOR dosage: unknown. During the same period patient was treated with AREDIA, VICODIN, ASPIRIN, NIASPAN, FOSAMAX, FLONASE, ATROVENT. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5629892-5
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Feb 11, 2008. Female patient, 93 years of age, weighting 126.0 lb, was diagnosed with multiple myeloma, anaemia and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anxiety, bacterial culture positive, biopsy bone abnormal, bone debridement, bone disorder, epistaxis, gingival bleeding, impaired healing, . ZOMETA dosage: unknown. During the same period patient was treated with PROCRIT. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5630392-7
ZOMETA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 12, 2008. Female patient was diagnosed with metastases to bone, multiple myeloma, pain, hypertension, gastrooesophageal reflux disease and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anaemia, asthenia, blood albumin decreased, blood calcium decreased, blood glucose increased, blood potassium decreased, bone debridement, bone disorder, . ZOMETA dosage: 4 MG EVERY 4 WEEKS. During the same period patient was treated with THALIDOMIDE, DEXAMETHASONE, FENTANYL, LISINOPRIL, ROXICODONE, PROTONIX. Patient was hospitalized. Patient recovered.
Pamidronate Side Effects Report #5631812-4
Health Professional from NETHERLANDS reported PAMIDRONATE DI problem on Feb 08, 2008. Female patient, 68 years of age, was diagnosed with metastases to bone and was treated with PAMIDRONATE DI. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone debridement, bone disorder, impaired healing, osteonecrosis, tooth extraction, . PAMIDRONATE DI dosage: unknown. Patient was hospitalized. Patient recovered.
Zoledronic Side Effects Report #5632945-9
ZOLEDRONIC ACID problem was reported by a Health Professional from UNITED KINGDOM on Feb 12, 2008. Female patient, 51 years of age, was diagnosed with metastases to bone and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, breath odour, dental caries, facial pain, jaw disorder, mouth ulceration, mucosal inflammation, nasal disorder, . ZOLEDRONIC ACID dosage: unknown. During the same period patient was treated with IBANDRONIC ACID, CLODRONATE DI, PAMIDRONATE DI. Patient recovered.
Zometa Side Effects Report #5638861-0
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Feb 18, 2008. Male patient, 49 years of age, was diagnosed with metastases to bone, non-small cell lung cancer stage iv and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, impaired healing, osteonecrosis, pain in jaw, . ZOMETA dosage: 4 MG, ONCE MONTHLY. During the same period patient was treated with DEXAMETHASONE, AVASTIN, TAXOTERE, ALIMTA, CARBOPLATIN. Patient recovered.
Zometa Side Effects Report #5641798-4
ZOMETA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 18, 2008. Female patient was diagnosed with metastases to bone, multiple myeloma, pain, hypertension, gastrooesophageal reflux disease and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anaemia, asthenia, blood albumin decreased, blood calcium decreased, blood glucose increased, blood potassium decreased, bone debridement, bone disorder, . ZOMETA dosage: 4 MG EVERY 4 WEEKS (MONTHLY). During the same period patient was treated with THALIDOMIDE, DEXAMETHASONE, FENTANYL, LISINOPRIL, ROXICODONE, PROTONIX. Patient was hospitalized. Patient recovered.
Thalomid Side Effects Report #5589309-6
Health Professional from PORTUGAL reported THALOMID problem on Jan 02, 2008. Male patient, 71 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, osteomyelitis bacterial, osteonecrosis, tooth extraction, . THALOMID dosage: 100 MG, DAILY, ORAL. During the same period patient was treated with DEXAMETHASONE, CYCLOPHOSPHAMIDE, ERYTHROPOIETIN, ZOLEDRONIC ACID. Patient recovered.
Thalomid Side Effects Report #5591055-X
THALOMID problem was reported by a Physician from PORTUGAL on Jan 02, 2008. Male patient, 66 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, osteomyelitis, osteonecrosis, tooth abscess, tooth extraction, . THALOMID dosage: 100 MG, DAILY, ORAL. During the same period patient was treated with DEXAMETHASONE, ZOLEDRONIC ACID, CYCLOPHOSPHAMIDE, ERYTHROPOETIN, AMOXICILLIN, NEUPOGEN. Patient recovered.
Aredia Side Effects Report #5595899-X
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Jan 15, 2008. Female patient, 69 years of age, weighting 129.2 lb, was diagnosed with breast cancer and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone debridement, bone disorder, bone operation, breath odour, chronic sinusitis, computerised tomogram abnormal, dental discomfort, depressed mood, . AREDIA dosage: 90MG IV Q3 WEEKS. During the same period patient was treated with ZOMETA, PRILOSEC, FEMARA, VALIUM, AROMASIN, XELODA. Patient recovered.
Paragard Side Effects Report #5619485-8
PARAGARD T problem was reported by a Physician from UNITED STATES on Sept 21, 2007. Female patient, 42 years of age, weighting 116.0 lb, was diagnosed with contraception, actinomycosis and was treated with PARAGARD T. After drug was administered, patient experienced the following problems/side effects: actinomycosis, coital bleeding, diarrhoea, fatigue, fungal infection, haemorrhagic ovarian cyst, oral candidiasis, uterine leiomyoma, . PARAGARD T dosage: unknown. During the same period patient was treated with PARAGARD T, PENICILLIN, OMEPRAZOLE. Patient recovered.
Zometa Side Effects Report #5553646-1
Physician from UNITED STATES reported ZOMETA problem on Dec 10, 2007. Male patient, 73 years of age, weighting 154.0 lb, was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, alpha haemolytic streptococcal infection, anxiety, inflammation, injury, osteomyelitis, osteonecrosis, pain, wound debridement, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA. Patient recovered.
Zometa Side Effects Report #5556889-6
ZOMETA problem was reported by a Physician from UNITED STATES on Dec 06, 2007. Female patient, 70 years of age, weighting 94.98 lb, was diagnosed with metastases to bone, spinal cord compression, breast cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, mucosal inflammation, osteonecrosis, primary sequestrum, resorption bone increased, sequestrectomy, tooth disorder, wound debridement, . ZOMETA dosage: 4 MG MONTHLY. During the same period patient was treated with AREDIA, DECADRON, XELODA, FASLODEX. Patient recovered.
Pepcid Side Effects Report #5564318-1
Physician from UNITED STATES reported PEPCID problem on Dec 14, 2007. Female patient, 77 years of age, was diagnosed with multiple myeloma, insomnia, depression and was treated with PEPCID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, alopecia, alveoloplasty, atelectasis, back pain, blood glucose increased, blood lactate dehydrogenase increased, bloody discharge, bone debridement, . PEPCID dosage: unknown. During the same period patient was treated with AREDIA, DECADRON, PREDNISONE, FAMVIR, MELPHALAN, XANAX, PAXIL, BACTRIM. Patient died.
Aredia Side Effects Report #5565937-9
AREDIA problem was reported by a Physician from UNITED STATES on Dec 14, 2007. Female patient, 70 years of age, weighting 126.0 lb, was diagnosed with metastases to bone, breast cancer, parkinson's disease and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, aortic arteriosclerosis, aortic valve incompetence, aphonia, bone debridement, bone disorder, calcinosis, cyst, cyst aspiration, . AREDIA dosage: unknown. During the same period patient was treated with CYTOXAN, FLUOROURACIL, ARIMIDEX, CALCIUM, CARBIDOPA, TIMOLOL MALEATE, ASPIRIN, GEMZAR. Patient was hospitalized. Patient died.
Zometa Side Effects Report #5503659-0
Physician from reported ZOMETA problem on Oct 25, 2007. Female patient, 61 years of age, was diagnosed with plasmacytoma, pyrexia and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, ageusia, apheresis, aspiration bone marrow, biopsy, bone disorder, candidiasis, catheterisation venous, computerised tomogram abnormal, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with IDARUBICIN, DEXAMETHASONE, PANTOPRAZOLE, COTRIM DS, TAZOBACTAM, MELPHALAN. Patient was hospitalized. Patient recovered.
Aredia Side Effects Report #5506330-4
AREDIA problem was reported by a Consumer or non-health professional from JAPAN on Oct 26, 2007. Female patient, 72 years of age, weighting 103.6 lb, was diagnosed with metastases to bone and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, c-reactive protein increased, erythema, fistula, oral pruritus, osteonecrosis, pain in jaw, swelling, tooth extraction, . AREDIA dosage: 90 MG, EVERY 4 WEEKS. During the same period patient was treated with BISPHONAL. Patient recovered.
Ferrous Side Effects Report #5512177-5
Consumer or non-health professional from UNITED STATES reported FERROUS SULPHATE problem on Nov 02, 2007. Female patient, 74 years of age, weighting 91.98 lb, was diagnosed with lung neoplasm malignant and was treated with FERROUS SULPHATE. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anaemia, biopsy bone abnormal, bone operation, breast cyst, diarrhoea, diverticulum, dry mouth, dry skin, . FERROUS SULPHATE dosage: 325 MG M-W-F. During the same period patient was treated with POTASSIUM CHLORIDE, NIFEDIPINE, TARCEVA, VITAMINS AND IRON, CALCIUM, MEGACE, AUGMENTIN, CARBOPLATIN W. Patient recovered.
Aredia Side Effects Report #5520953-8
AREDIA problem was reported by a Consumer or non-health professional from JAPAN on Nov 14, 2007. Female patient, 72 years of age, weighting 103.6 lb, was diagnosed with metastases to bone and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, c-reactive protein increased, erythema, fistula, oral pruritus, osteonecrosis, pain in jaw, swelling, . AREDIA dosage: 90 MG, EVERY 4 WEEKS. During the same period patient was treated with BISPHONAL. Patient recovered.
Ferrous Side Effects Report #5524475-X
Consumer or non-health professional from UNITED STATES reported FERROUS SULPHATE problem on Nov 12, 2007. Female patient, 74 years of age, weighting 91.98 lb, was diagnosed with lung neoplasm malignant and was treated with FERROUS SULPHATE. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anaemia, biopsy bone abnormal, bone operation, breast cyst, breath sounds abnormal, diarrhoea, diverticulum, dry mouth, . FERROUS SULPHATE dosage: 325 MG M-W-F. During the same period patient was treated with POTASSIUM CHLORIDE, NIFEDIPINE, TARCEVA, VITAMINS AND IRON, CALCIUM, MEGACE, AUGMENTIN, CARBOPLATIN W. Patient recovered.
Zometa Side Effects Report #5524483-9
ZOMETA problem was reported by a Health Professional from BELGIUM on Nov 14, 2007. Male patient, 57 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, impaired healing, osteitis, osteonecrosis, purulent discharge, tooth extraction, wound debridement, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA, ANTIHYPERTENSIVES. Patient recovered.
Fosamax Side Effects Report #5582049-9
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on June 12, 2007. Female patient, 63 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinomycosis, osteonecrosis, . FOSAMAX dosage: 70 MG/PO. During the same period patient was treated with SYNTHROID, LITHIUM CARBONATE. Patient recovered.
Prednisone Side Effects Report #5484832-7
PREDNISONE problem was reported by a Physician from UNITED KINGDOM on Sept 25, 2007. Female patient, 33 years of age, was diagnosed with colitis ulcerative and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: actinomycosis, breast abscess, breast cellulitis, impaired healing, . PREDNISONE dosage: 5 MG; QD;. During the same period patient was treated with ORAPRED. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5491486-2
Consumer or non-health professional from JAPAN reported ZOMETA problem on Oct 12, 2007. Female patient, 70 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, neutrophil count increased, osteonecrosis, pain in jaw, periodontitis, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with AREDIA, HERCEPTIN, DOCETAXEL. Patient was hospitalized. Patient recovered.
Aredia Side Effects Report #5494176-5
AREDIA problem was reported by a Physician from UNITED STATES on Oct 16, 2007. Male patient, 71 years of age, weighting 178.0 lb, was diagnosed with metastases to bone and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, biopsy, bone disorder, bone erosion, bone fragmentation, computerised tomogram abnormal, dental treatment, exostosis, fall, . AREDIA dosage: unknown. During the same period patient was treated with ZOMETA, PROCRIT, IRON SUPPLEMENTS, NEURONTIN, FOLIC ACID, BUMEX, NAPROXEN. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5501290-4
Physician from UNITED STATES reported FOSAMAX problem on Oct 23, 2007. Female patient, 75 years of age, weighting 143.3 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anxiety, bronchitis, cardiac disorder, chronic obstructive pulmonary disease, compression fracture, condition aggravated, coronary artery disease, depression, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5444635-6
FOSAMAX problem was reported by a Physician from UNITED STATES on Aug 30, 2007. Female patient, 74 years of age, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinomycosis, adverse event, anxiety, oedema peripheral, osteomyelitis, osteonecrosis, postmenopausal haemorrhage, transient ischaemic attack, . FOSAMAX dosage: unknown. During the same period patient was treated with THALIDOMIDE. Patient was hospitalized and became disabled. Patient recovered.
Pamidronate Side Effects Report #5449339-1
Physician from UNITED KINGDOM reported PAMIDRONATE DI problem on Aug 30, 2007. Female patient, 51 years of age, was diagnosed with metastases to bone, breast cancer and was treated with PAMIDRONATE DI. After drug was administered, patient experienced the following problems/side effects: actinomycosis, breath odour, dental alveolar anomaly, dental caries, inflammation, mucosal ulceration, nasal disorder, osteonecrosis, . PAMIDRONATE DI dosage: unknown. During the same period patient was treated with METHOTREXATE, FLUOROURACIL, CLODRONATE, ZOLEDRONIC ACID, IBANDRONATE, TAMOXIFEN CITRATE, EXEMESTANE, ANASTROZOLE. Patient recovered.
Zometa Side Effects Report #5404884-X
ZOMETA problem was reported by a Consumer or non-health professional from GERMANY on July 27, 2007. Male patient, 61 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, dental fistula, dental treatment, impaired healing, inflammation, oral surgery, osteitis, osteomyelitis, osteonecrosis, . ZOMETA dosage: unknown. During the same period patient was treated with CIBACEN, METOPROLOL SUCCINATE, IBUHEXAL, GLIMEPIRIDE. Patient recovered.
Zoledronic Side Effects Report #5409275-3
Health Professional from UNITED STATES reported ZOLEDRONIC ACID problem on Aug 02, 2007. Female patient, 58 years of age, was diagnosed with breast cancer metastatic and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone disorder, breast cancer, contrast media reaction, inflammation, oedema mouth, oral pain, oral torus, osteomyelitis, . ZOLEDRONIC ACID dosage: 4 MG EVERY 3 TO 4 WEEKS. During the same period patient was treated with CAPECITABINE, IXABEPILONE, PREDNISONE, CHLORHEXIDINE GLUCONATE. Patient recovered.
Femara Side Effects Report #5413228-9
FEMARA problem was reported by a Physician from GERMANY on Aug 08, 2007. Female patient, 59 years of age, weighting 110.2 lb, was diagnosed with breast cancer female, pain, metastases to bone and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, biopsy bone abnormal, bone disorder, chronic sinusitis, fistula, impaired healing, inflammation, oral surgery, osteonecrosis, . FEMARA dosage: 2.5 MG, QD. During the same period patient was treated with VALORON N, VIOXX, BERLOSIN, ZOMETA, TAXOTERE. Patient recovered.
Pamidronate Side Effects Report #5414855-5
Physician from GERMANY reported PAMIDRONATE DI problem on Aug 08, 2007. Female patient, 73 years of age, weighting 187.4 lb, was diagnosed with metastases to bone and was treated with PAMIDRONATE DI. After drug was administered, patient experienced the following problems/side effects: actinomycosis, biopsy bone abnormal, oral surgery, osteonecrosis, osteotomy, periodontitis, primary sequestrum, scintigraphy, single photon emission computerised tomogram abnormal, . PAMIDRONATE DI dosage: 90 MG, QMO. During the same period patient was treated with ZOMETA. Patient recovered.
Zometa Side Effects Report #5415337-7
ZOMETA problem was reported by a Physician from on Aug 07, 2007. Female patient, 61 years of age, was diagnosed with plasmacytoma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, biopsy, bone disorder, computerised tomogram abnormal, condition aggravated, fistula, histology abnormal, hyperplasia, . ZOMETA dosage: 4 MG, QMO. Patient recovered.
Zometa Side Effects Report #5416366-X
Consumer or non-health professional from GERMANY reported ZOMETA problem on Aug 10, 2007. Female patient, 80 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, biopsy bone abnormal, bone disorder, excessive granulation tissue, osteitis, osteonecrosis, periodontitis, sequestrectomy, tooth extraction, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with CLINDAMYCIN, CORDANUM, LISIHEXAL, XELODA. Patient recovered.
Aredia Side Effects Report #5416387-7
AREDIA problem was reported by a Consumer or non-health professional from GERMANY on Aug 10, 2007. Female patient, 64 years of age, was diagnosed with multiple myeloma and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, histology abnormal, jaw disorder, oral surgery, osteonecrosis, scintigraphy, tooth extraction, x-ray dental, . AREDIA dosage: unknown. During the same period patient was treated with CLINDAMYCIN, ASPIRIN, LISIHEXAL, CALCILAC KT, MAREEN, PENTAERYTHRITOL TETRANITRATE, QUERTO. Patient recovered.
Aredia Side Effects Report #5427166-9
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Aug 20, 2007. Female patient, 44 years of age, weighting 249.0 lb, was diagnosed with metastases to bone and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, artificial crown procedure, bone lesion, breast cancer metastatic, dental caries, excessive granulation tissue, fistula, osteitis, osteonecrosis, . AREDIA dosage: unknown. During the same period patient was treated with ZOMETA. Patient recovered.
Fosamax Side Effects Report #5440817-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Aug 22, 2007. Female patient, 75 years of age, weighting 143.3 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinomycosis, anxiety, bronchitis, cardiac disorder, chronic obstructive pulmonary disease, compression fracture, coronary artery disease, depression, insomnia, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5375864-8
Physician from GERMANY reported ZOMETA problem on June 22, 2007. Female patient, 75 years of age, was diagnosed with osteopenia, plasmacytoma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: actinomycosis, acute sinusitis, amnesia, antibiotic prophylaxis, biopsy, blood creatinine increased, blood immunoglobulin a increased, bone disorder, cellulitis, . ZOMETA dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, ALKERAN. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5379436-0
FOSAMAX problem was reported by a Physician from UNITED STATES on June 29, 2007. Female patient, 74 years of age, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinomycosis, adverse event, anxiety, oedema peripheral, osteomyelitis, osteonecrosis, transient ischaemic attack, . FOSAMAX dosage: unknown. During the same period patient was treated with THALIDOMIDE. Patient was hospitalized and became disabled. Patient recovered.
Prednisolone Side Effects Report #5379651-6
Physician from AUSTRALIA reported PREDNISOLONE problem on June 25, 2007. Male patient, 52 years of age, was diagnosed with multiple myeloma and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: actinomycosis, bone debridement, granuloma, impaired healing, oral disorder, oral pain, osteonecrosis, sepsis, tooth extraction, . PREDNISOLONE dosage: 25 MG, EVERY 48 HOURS. During the same period patient was treated with THALIDOMIDE, ZOLEDRONIC ACID. Patient recovered.