GINGIVAL ULCERATION side effect
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Drugs associated with GINGIVAL ULCERATION
ACTOS AVASTIN BYETTA CHANTIX CREST ETHEDENT FENTORA FOSAMAX HUMIRA LISTERINE NAPROSYN PAMIDRONATE PANTOPRAZOLE SOFTMINT ZOMETAFosamax Side Effects Report #5572600-7
Physician from UNITED STATES reported FOSAMAX problem on Feb 23, 2007. Female patient, 76 years of age, weighting 149.0 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gingival ulceration, osteonecrosis, . FOSAMAX dosage: 70 MG WKY PO. During the same period patient was treated with CALTRATE, MOBIC, VIOXX, ZOCOR, DOCUSATE, GASTROINTESTINAL PREPARATIONS, VITAMINS, ZOLPIDEM TARTRATE. Patient recovered.
Avastin Side Effects Report #5502301-2
AVASTIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 16, 2007. Female patient, 55 years of age, weighting 340.2 lb, was diagnosed with breast cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: gingival ulceration, osteonecrosis, . AVASTIN dosage: 15 MG/ML, UNK. During the same period patient was treated with ZOMETA, TAXOTERE, ZOFRAN. Patient recovered.
Avastin Side Effects Report #5468778-6
Physician from UNITED KINGDOM reported AVASTIN problem on Sept 11, 2007. Female patient, 60 years of age, was diagnosed with breast cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: gingival ulceration, . AVASTIN dosage: unknown. During the same period patient was treated with ZOMETA. Patient recovered.
Zometa Side Effects Report #5778816-9
ZOMETA problem was reported by a Physician from FRANCE on June 17, 2008. Male patient, weighting 132.3 lb, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: gingival ulceration, malignant neoplasm progression, osteonecrosis, tooth resorption, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with TARCEVA. Patient died on 05/28/2008.
Fosamax Side Effects Report #5662923-5
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Mar 03, 2008. 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: arthropathy, gingival ulceration, osteomyelitis, osteonecrosis, temporomandibular joint syndrome, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Pantoprazole Side Effects Report #5628524-X
PANTOPRAZOLE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 14, 2008. Female patient, 68 years of age, weighting 121.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PANTOPRAZOLE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, gingival ulceration, mouth ulceration, pharyngeal ulceration, tongue ulceration, . PANTOPRAZOLE dosage: 40 MG TAB ONE PER DAY PO. Patient recovered.
Zometa Side Effects Report #5598109-2
Consumer or non-health professional from FRANCE reported ZOMETA problem on Jan 14, 2008. Male patient, 87 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: bone density decreased, gingival ulceration, osteonecrosis, pain in jaw, . ZOMETA dosage: 4 MG EVERY 4 WEEKS. During the same period patient was treated with CLASTOBAN, ANANDRON, DECAPEPTYL. Patient was hospitalized. Patient recovered.
Ethedent Side Effects Report #5563248-9
ETHEDENT RM SPEARMINT problem was reported by a Health Professional from UNITED STATES on Dec 14, 2007. Female patient, weighting 155.0 lb, was diagnosed with dental disorder prophylaxis and was treated with ETHEDENT RM SPEARMINT. After drug was administered, patient experienced the following problems/side effects: gingival pain, gingival ulceration, . ETHEDENT RM SPEARMINT dosage: unknown. Patient recovered.
Byetta Side Effects Report #5575933-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 09, 2007. Female patient, 60 years of age, was diagnosed with insulin-requiring type ii diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: gingival bleeding, gingival ulceration, stomatitis, . BYETTA dosage: unknown. During the same period patient was treated with NOVOLIN, GLUCOPHAGE. Patient recovered.
Softmint Side Effects Report #5492688-1
SOFTMINT SENSATION LISTERINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 03, 2007. Female patient was diagnosed with dental plaque and was treated with SOFTMINT SENSATION LISTERINE. After drug was administered, patient experienced the following problems/side effects: gingival blister, gingival ulceration, mouth ulceration, oedema mouth, oral intake reduced, oral mucosal blistering, oral pain, . SOFTMINT SENSATION LISTERINE dosage: unknown. Patient recovered.
Listerine Side Effects Report #5493055-7
Consumer or non-health professional from UNITED STATES reported LISTERINE AGENT COOL BLUE BUBBLE BLAST problem on Oct 08, 2007. Female patient was diagnosed with dental disorder prophylaxis and was treated with LISTERINE AGENT COOL BLUE BUBBLE BLAST. After drug was administered, patient experienced the following problems/side effects: gingival bleeding, gingival ulceration, . LISTERINE AGENT COOL BLUE BUBBLE BLAST dosage: 10 ML 1 TIME PER DAY; ORAL. Patient recovered.
Listerine Side Effects Report #5500310-0
LISTERINE WHITENING QUICK DISSOLVING STRIPS problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2007. Female patient was treated with LISTERINE WHITENING QUICK DISSOLVING STRIPS. After drug was administered, patient experienced the following problems/side effects: crying, gingival ulceration, panic disorder, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. Patient recovered.
Naprosyn Side Effects Report #5439513-2
Health Professional from UNITED KINGDOM reported NAPROSYN problem on Aug 20, 2007. Male patient, 20 years of age, weighting 172.0 lb, was treated with NAPROSYN. After drug was administered, patient experienced the following problems/side effects: chapped lips, gingival ulceration, lip swelling, mouth ulceration, . NAPROSYN dosage: unknown. Patient recovered.
Humira Side Effects Report #5770452-3
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 30, 2008. Female patient, weighting 143.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: ear infection, gingival ulceration, sinusitis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.
Listerine Side Effects Report #5717141-9
Physician from UNITED STATES reported LISTERINE AGENT COOL BLUE BUBBLE BLAST problem on Apr 15, 2008. Female patient, 40 years of age, was diagnosed with dental disorder prophylaxis and was treated with LISTERINE AGENT COOL BLUE BUBBLE BLAST. After drug was administered, patient experienced the following problems/side effects: gingival bleeding, gingival ulceration, . LISTERINE AGENT COOL BLUE BUBBLE BLAST dosage: 10 ML 1 TIME PER DAY (1 IN 1 D),ORAL. Patient recovered.
Fosamax Side Effects Report #5718075-6
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 16, 2008. 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: arthropathy, gingival ulceration, osteomyelitis, osteonecrosis, temporomandibular joint syndrome, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5298905-5
Physician from GERMANY reported ZOMETA problem on Apr 04, 2007. Female patient, 64 years of age, weighting 149.9 lb, was diagnosed with metastases to bone, breast cancer and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: dental treatment, gingival ulceration, impaired healing, jaw disorder, jaw lesion excision, osteonecrosis, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with NAVELBINE. Patient recovered.
Zometa Side Effects Report #5254088-9
ZOMETA problem was reported by a Physician from AUSTRIA on Feb 19, 2007. Female patient, 76 years of age, was diagnosed with multiple myeloma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone disorder, gingival ulceration, jaw operation, osteonecrosis, . ZOMETA dosage: 4 MG, ONCE MONTHLY. Patient recovered.
Listerine Side Effects Report #5616101-6
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING QUICK DISSOLVING STRIPS problem on Jan 23, 2008. Female patient was diagnosed with dental care and was treated with LISTERINE WHITENING QUICK DISSOLVING STRIPS. After drug was administered, patient experienced the following problems/side effects: caustic injury, gingival pain, gingival ulceration, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. Patient recovered.
Fentora Side Effects Report #5483525-X
FENTORA problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2007. Female patient, 48 years of age, weighting 178.0 lb, was diagnosed with back pain, migraine and was treated with FENTORA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site ulcer, gingival ulceration, incorrect dose administered, mouth ulceration, somnolence, tongue haemorrhage, tongue ulceration, . FENTORA dosage: unknown. Patient recovered.
Zometa Side Effects Report #5485160-6
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Oct 08, 2007. Male patient, 66 years of age, weighting 224.0 lb, was diagnosed with multiple myeloma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood product transfusion, bone disorder, gingival ulceration, hallucination, loose tooth, mental status changes, osteonecrosis, renal impairment, soft tissue inflammation, . ZOMETA dosage: unknown. During the same period patient was treated with THALIDOMIDE, ALLOPURINOL, CELEBREX, ALLEGRA, INTERFERON. Patient recovered.
Actos Side Effects Report #5390948-6
ACTOS problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, weighting 102.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: angina pectoris, anorexia, gingival ulceration, oedema mouth, oral discomfort, pharyngolaryngeal pain, scab, . ACTOS dosage: unknown. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5390948-6
Consumer or non-health professional from UNITED STATES reported ACTOS problem on July 05, 2007. Female patient, weighting 102.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: angina pectoris, anorexia, gingival ulceration, oedema mouth, oral discomfort, pharyngolaryngeal pain, scab, . ACTOS dosage: unknown. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5785972-5
ZOMETA problem was reported by a Health Professional from UNITED STATES on June 17, 2008. Female patient, weighting 166.0 lb, was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone disorder, bone lesion, gingival ulceration, oral pain, osteolysis, osteonecrosis, pain in jaw, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with TAXOL, AVASTIN. Patient recovered.
Crest Side Effects Report #5734399-0
Consumer or non-health professional from UNITED STATES reported CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR problem on May 08, 2008. Female patient, 39 years of age, weighting 159.0 lb, was diagnosed with dental plaque, gingivitis, prophylaxis and was treated with CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR. After drug was administered, patient experienced the following problems/side effects: fluid intake reduced, gingival disorder, gingival ulceration, jaw disorder, oral intake reduced, oral pain, stomatitis, . CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR dosage: unknown. During the same period patient was treated with CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR, CREST PRO HEALTH MOUTHWASH NIGHT NORMAL PROCTOR. Patient recovered.
Zometa Side Effects Report #5737223-5
ZOMETA problem was reported by a Consumer or non-health professional from GREECE on May 05, 2008. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone disorder, gingival swelling, gingival ulceration, impaired healing, mastication disorder, metastasis, no adverse event, osteomyelitis, . ZOMETA dosage: unknown. Patient was hospitalized. Patient recovered.
Chantix Side Effects Report #5741203-3
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on May 08, 2008. Female patient, weighting 164.9 lb, was diagnosed with thyroid disorder and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: dysgeusia, gingival bleeding, gingival ulceration, oral pain, sputum discoloured, stomatitis, . CHANTIX dosage: unknown. During the same period patient was treated with LEVOXYL. Patient recovered.
Pamidronate Side Effects Report #5697393-4
PAMIDRONATE DI problem was reported by a Health Professional from UNITED STATES on Mar 27, 2008. Female patient, 65 years of age, was diagnosed with multiple myeloma and was treated with PAMIDRONATE DI. After drug was administered, patient experienced the following problems/side effects: gingival erythema, gingival swelling, gingival ulceration, impaired healing, osteonecrosis, tooth extraction, tooth fracture, . PAMIDRONATE DI dosage: 90 MG PER MONTH. During the same period patient was treated with ZOLEDRONIC ACID, THALIDOMIDE, DEXAMETHASONE. Patient recovered.