GINGIVAL DISORDER side effect
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Drugs associated with GINGIVAL DISORDER
ACTONEL ACTOS ALTACE ARAVA AREDIA BIAXIN BONIVA BOTOX CHANTIX COMMIT COMTESS CREST CRESTOR CYMBALTA DACTINOMYCIN DIDROCAL DILANTIN FENTORA FORTEO FOSAMAX HYDROGEN IRESSA KAREWAY LAMICTAL LISTERINE LOTREL LUNESTA NEXIUM NICORETTE NICOTROL ORAJEL OXYCONTIN PEGASYS PLENDIL PULMICORT REBIF REVLIMID RITUXIMAB THALIDOMIDE THALOMID TYSABRI WHITENING ZOLEDRONIC ZOMETAFosamax Side Effects Report #5662298-1
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Mar 03, 2008. Female patient, 53 years of age, was diagnosed with osteoporosis, hip fracture and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gingival disorder, hip fracture, lower limb fracture, osteonecrosis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Thalidomide Side Effects Report #5672374-5
THALIDOMIDE problem was reported by a Physician from UNITED STATES on Mar 12, 2008. Female patient, 60 years of age, was diagnosed with hypercalcaemia of malignancy and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: gingival disorder, osteonecrosis, tooth extraction, . THALIDOMIDE dosage: unknown. During the same period patient was treated with DEXAMETHASONE, ZOMETA. Patient recovered.
Altace Side Effects Report #5672775-5
Pharmacist from UNITED STATES reported ALTACE problem on Nov 08, 2007. Female patient was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: gingival disorder, . ALTACE dosage: 5 MG, QD. During the same period patient was treated with TENEX. Patient recovered.
Plendil Side Effects Report #5632426-2
PLENDIL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Female patient, 61 years of age, weighting 160.1 lb, was treated with PLENDIL. After drug was administered, patient experienced the following problems/side effects: gingival disorder, tooth disorder, . PLENDIL dosage: unknown. During the same period patient was treated with VITAMIN CAP. Patient recovered.
Revlimid Side Effects Report #5647120-1
Physician from UNITED STATES reported REVLIMID problem on Dec 04, 2007. Male patient, 55 years of age, was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: gingival disorder, . REVLIMID dosage: 25 MG, DAILY X 21 DAYS, ORAL. Patient recovered.
Commit Side Effects Report #5516318-5
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2007. Female patient, 31 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: gingival disorder, gingival pain, oral pain, . COMMIT dosage: unknown. Patient recovered.
Thalomid Side Effects Report #5489229-1
Physician from UNITED STATES reported THALOMID problem on Oct 10, 2007. Female patient, 57 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: gingival disorder, impaired healing, . THALOMID dosage: 200 MG, 4 IN 1 D, ORAL; 100 MG, 2 IN 1 D. Patient recovered.
Thalomid Side Effects Report #5455512-9
THALOMID problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 10, 2007. Female patient, 57 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: gingival disorder, impaired healing, . THALOMID dosage: 200 MG, 4 IN 1 D, ORAL; 100 MG, 2 IN 1 D. Patient recovered.
Forteo Side Effects Report #5422594-X
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Aug 09, 2007. Female patient, 60 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: gingival disorder, mouth ulceration, oral pain, salivary gland cancer, salivary gland mass, tooth injury, . FORTEO dosage: unknown. Patient recovered.
Nicorette Side Effects Report #5388078-2
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 06, 2006. Female patient, 55 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: gingival disorder, insomnia, . NICORETTE dosage: unknown. Patient recovered.
Boniva Side Effects Report #5403040-9
Consumer or non-health professional from UNITED STATES reported BONIVA problem on Apr 12, 2007. Female patient, 61 years of age, was diagnosed with prophylaxis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: gingival disorder, osteonecrosis, . BONIVA dosage: 150 MG 1 PER MONTH ORAL. During the same period patient was treated with WELLBUTRIN, VITAMINS NOS, CALCIUM NOS. Patient recovered.
Nicorette Side Effects Report #5388078-2
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 06, 2006. Female patient, 55 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: gingival disorder, insomnia, . NICORETTE dosage: unknown. Patient recovered.
Boniva Side Effects Report #5403040-9
Consumer or non-health professional from UNITED STATES reported BONIVA problem on Apr 12, 2007. Female patient, 61 years of age, was diagnosed with prophylaxis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: gingival disorder, osteonecrosis, . BONIVA dosage: 150 MG 1 PER MONTH ORAL. During the same period patient was treated with WELLBUTRIN, VITAMINS NOS, CALCIUM NOS. Patient recovered.
Zometa Side Effects Report #5785971-3
ZOMETA problem was reported by a Physician from JAPAN on June 16, 2008. Male patient, weighting 116.8 lb, was diagnosed with bone lesion and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: gingival disorder, jaw disorder, osteonecrosis, . ZOMETA dosage: 4 MG/DAY. During the same period patient was treated with DECADRON, ITRIZOLE, RABEPRAZOLE, BAKTAR, ALOSITOL, AZUCURENIN S, MAGNESIUM OXIDE, CALCIUM POLYSTYRENE SULFONATE. Patient recovered.
Fosamax Side Effects Report #5728281-2
Health Professional from UNITED STATES reported FOSAMAX problem on May 02, 2008. Female patient, 60 years of age, weighting 93.00 lb, was diagnosed with osteoporosis prophylaxis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gingival disorder, impaired healing, osteonecrosis, palatal disorder, . FOSAMAX dosage: unknown. Patient recovered.
Zometa Side Effects Report #5333131-2
ZOMETA problem was reported by a Physician from UNITED STATES on May 21, 2007. Female patient, 54 years of age, weighting 189.0 lb, was diagnosed with breast cancer and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: gingival disorder, osteonecrosis, . ZOMETA dosage: 4.3 MG MONTHLY IV. Patient recovered.
Crestor Side Effects Report #5237116-6
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on Apr 07, 2005. Female patient was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: gingival disorder, gingival pain, . CRESTOR dosage: 20 MG PO. Patient recovered.
Fosamax Side Effects Report #5262684-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 02, 2007. Female patient, 59 years of age, weighting 189.6 lb, was diagnosed with osteoporosis, spinal compression fracture and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: gingival disorder, gingival recession, osteonecrosis, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, EFFEXOR, CARDIZEM CD, GUAIFENESIN, DAYPRO. Patient recovered.
Fosamax Side Effects Report #5622079-1
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Jan 31, 2008. Female patient, 38 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: cervix carcinoma, gingival disorder, osteonecrosis, pain, pain management, rheumatoid arthritis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Didrocal Side Effects Report #5640849-0
DIDROCAL problem was reported by a Consumer or non-health professional from CANADA on Feb 19, 2008. Female patient, 79 years of age, was diagnosed with osteoporosis and was treated with DIDROCAL. After drug was administered, patient experienced the following problems/side effects: dysgeusia, gingival disorder, impaired healing, loose tooth, tongue disorder, tooth extraction, . DIDROCAL dosage: unknown. Patient recovered.
Biaxin Side Effects Report #5604628-2
Consumer or non-health professional from CANADA reported BIAXIN problem on Jan 24, 2008. Female patient, weighting 165.3 lb, was diagnosed with dermal cyst and was treated with BIAXIN. After drug was administered, patient experienced the following problems/side effects: dry mouth, gingival disorder, tongue dry, . BIAXIN dosage: 2 CO OF 500 MG ONCE A DAY PO. Patient recovered.
Zometa Side Effects Report #5572864-X
ZOMETA problem was reported by a Consumer or non-health professional from ITALY on Dec 19, 2007. Male patient was diagnosed with multiple myeloma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone debridement, gingival disorder, osteonecrosis, pain in jaw, surgery, tooth extraction, tooth fracture, . ZOMETA dosage: 4 MG, UNK. Patient recovered.
Fosamax Side Effects Report #5574652-7
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Dec 26, 2007. Female patient, 59 years of age, weighting 158.0 lb, was diagnosed with bone density decreased and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone disorder, gingival disorder, gingival pain, impaired healing, osteonecrosis, . FOSAMAX dosage: 35 MG ONCE A WEEK. Patient recovered.
Oxycontin Side Effects Report #5504103-X
OXYCONTIN problem was reported by a Consumer or non-health professional from on Oct 18, 2007. Female patient was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: dental caries, gingival disorder, tooth loss, . OXYCONTIN dosage: UNK MG, UNK. Patient recovered.
Oxycontin Side Effects Report #5522159-5
Consumer or non-health professional from UNITED STATES reported OXYCONTIN problem on Nov 08, 2007. Female patient was diagnosed with spinal osteoarthritis and was treated with OXYCONTIN. After drug was administered, patient experienced the following problems/side effects: dental caries, gingival disorder, tooth loss, . OXYCONTIN dosage: UNK MG, UNK. During the same period patient was treated with DIAZEPAM, ESTROGEN, MOTRIN, MS CONTIN. Patient recovered.
Lunesta Side Effects Report #5494643-4
LUNESTA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 16, 2007. Female patient, 71 years of age, weighting 145.0 lb, was diagnosed with insomnia and was treated with LUNESTA. After drug was administered, patient experienced the following problems/side effects: gingival disorder, glossitis, middle insomnia, palatal disorder, . LUNESTA dosage: 3 MG;HS;ORAL. Patient recovered.
Listerine Side Effects Report #5502841-6
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING QUICK DISSOLVING STRIPS problem on Oct 17, 2007. Female patient, 32 years of age, was diagnosed with dental disorder prophylaxis and was treated with LISTERINE WHITENING QUICK DISSOLVING STRIPS. After drug was administered, patient experienced the following problems/side effects: caustic injury, gingival disorder, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. Patient recovered.
Nicotrol Side Effects Report #5446547-0
NICOTROL problem was reported by a Physician from SWEDEN on Aug 27, 2007. Female patient was diagnosed with cerebrovascular accident, chronic obstructive pulmonary disease and was treated with NICOTROL. After drug was administered, patient experienced the following problems/side effects: dependence, gingival disorder, total lung capacity decreased, . NICOTROL dosage: unknown. During the same period patient was treated with LIPITOR, TROMBYL, BRICANYL, SPIRIVA, ANTICOAGULANTS. Patient recovered.
Listerine Side Effects Report #5464029-7
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING QUICK DISSOLVING STRIPS problem on Sept 11, 2007. Female patient was diagnosed with dental disorder prophylaxis and was treated with LISTERINE WHITENING QUICK DISSOLVING STRIPS. After drug was administered, patient experienced the following problems/side effects: caustic injury, gingival disorder, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. Patient recovered.
Zometa Side Effects Report #5404886-3
ZOMETA problem was reported by a Health Professional from GERMANY on July 27, 2007. Female patient, 79 years of age, was diagnosed with multiple myeloma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: breath odour, gingival disorder, impaired healing, jaw operation, oral pain, osteonecrosis, periodontitis, primary sequestrum, tooth extraction, . ZOMETA dosage: unknown. Patient recovered.
Nicotrol Side Effects Report #5425716-X
Physician from SWEDEN reported NICOTROL problem on Aug 14, 2007. Female patient was diagnosed with cerebrovascular accident, chronic obstructive pulmonary disease and was treated with NICOTROL. After drug was administered, patient experienced the following problems/side effects: dependence, gingival disorder, total lung capacity decreased, . NICOTROL dosage: unknown. During the same period patient was treated with LIPITOR, TROMBYL, BRICANYL, SPIRIVA, ANTICOAGULANTS. Patient recovered.
Pegasys Side Effects Report #5396792-8
PEGASYS problem was reported by a Physician from CHINA on May 20, 2007. Female patient, 46 years of age, was diagnosed with hepatitis c and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: eye swelling, gingival disorder, photophobia, suicide attempt, . PEGASYS dosage: unknown. Patient recovered.
Kareway Side Effects Report #5397729-8
Consumer or non-health professional from UNITED STATES reported KAREWAY FLUORIDE ANTICAVITY TOOTHPASETE KAREWAY problem on July 23, 2007. Female patient, 57 years of age, weighting 185.0 lb, was treated with KAREWAY FLUORIDE ANTICAVITY TOOTHPASETE KAREWAY. After drug was administered, patient experienced the following problems/side effects: dental implantation, gingival disorder, impaired healing, implant site haemorrhage, implant site reaction, open wound, . KAREWAY FLUORIDE ANTICAVITY TOOTHPASETE KAREWAY dosage: unknown. Patient recovered.
Pegasys Side Effects Report #5396792-8
PEGASYS problem was reported by a Physician from CHINA on May 20, 2007. Female patient, 46 years of age, was diagnosed with hepatitis c and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: eye swelling, gingival disorder, photophobia, suicide attempt, . PEGASYS dosage: unknown. Patient recovered.
Kareway Side Effects Report #5397729-8
Consumer or non-health professional from UNITED STATES reported KAREWAY FLUORIDE ANTICAVITY TOOTHPASETE KAREWAY problem on July 23, 2007. Female patient, 57 years of age, weighting 185.0 lb, was treated with KAREWAY FLUORIDE ANTICAVITY TOOTHPASETE KAREWAY. After drug was administered, patient experienced the following problems/side effects: dental implantation, gingival disorder, impaired healing, implant site haemorrhage, implant site reaction, open wound, . KAREWAY FLUORIDE ANTICAVITY TOOTHPASETE KAREWAY dosage: unknown. Patient recovered.
Aredia Side Effects Report #5759071-2
AREDIA problem was reported by a Health Professional from UNITED STATES on May 28, 2008. Male patient was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: bone disorder, gingival disorder, impaired healing, osteonecrosis, tooth extraction, . AREDIA dosage: unknown. During the same period patient was treated with ZOMETA. Patient recovered.
Lamictal Side Effects Report #5773915-X
Physician from FRANCE reported LAMICTAL problem on June 06, 2008. Male patient was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: gingival atrophy, gingival disorder, sleep disorder, tooth loss, . LAMICTAL dosage: 400MG PER DAY. Patient recovered.
Listerine Side Effects Report #5775405-7
LISTERINE ANTISEPTIC MOUTHWASH problem was reported by a Consumer or non-health professional from UNITED STATES on June 06, 2008. Female patient, 38 years of age, weighting 220.0 lb, was diagnosed with dental disorder prophylaxis and was treated with LISTERINE ANTISEPTIC MOUTHWASH. After drug was administered, patient experienced the following problems/side effects: application site burn, gingival disorder, oral discomfort, thermal burn, . LISTERINE ANTISEPTIC MOUTHWASH dosage: unknown. During the same period patient was treated with PAMPRIN. Patient recovered.
Rituximab Side Effects Report #5782983-0
Health Professional from UNITED STATES reported RITUXIMAB problem on June 19, 2008. Female patient, weighting 145.0 lb, was diagnosed with mantle cell lymphoma and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: febrile neutropenia, gingival disorder, infection, . RITUXIMAB dosage: 640 MG IV. Patient recovered.
Pulmicort Side Effects Report #5786590-5
PULMICORT RESPULES problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2007. Female patient, 32 years of age, weighting 383.6 lb, was diagnosed with asthma and was treated with PULMICORT RESPULES. After drug was administered, patient experienced the following problems/side effects: gingival discolouration, gingival disorder, gingival swelling, . PULMICORT RESPULES dosage: unknown. During the same period patient was treated with SINGULAIR, NASONEX, DUONEB, ADVAIR DISKUS. Patient recovered.
Zoledronic Side Effects Report #5792134-4
Health Professional from UNITED STATES reported ZOLEDRONIC ACID problem on June 12, 2008. Female patient, 61 years of age, was diagnosed with metastases to bone, breast cancer metastatic and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: arthralgia, gingival disorder, headache, osteonecrosis, tooth extraction, . ZOLEDRONIC ACID dosage: 4 MG, Q3W. During the same period patient was treated with FLUOROPYRIMIDINE. Patient recovered.
Fosamax Side Effects Report #5731055-X
FOSAMAX problem was reported by a Health Professional from UNITED STATES on May 01, 2008. Female patient, 62 years of age, was diagnosed with osteoporosis, hypothyroidism and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: diverticulitis, gingival disorder, gingival recession, oral infection, tooth fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with LEVOXYL. Patient was hospitalized. 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.
Fosamax Side Effects Report #5735015-4
FOSAMAX problem was reported by a Health Professional from UNITED STATES on May 07, 2008. Female patient, 62 years of age, was diagnosed with osteoporosis, hypothyroidism and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: diverticulitis, gingival disorder, gingival recession, oral infection, tooth fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with LEVOXYL. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5742451-9
Consumer or non-health professional from UNITED STATES reported FOSAMAX PLUS D problem on Jan 10, 2008. Female patient, 47 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX PLUS D. After drug was administered, patient experienced the following problems/side effects: gingival bleeding, gingival disorder, oral disorder, oral infection, osteonecrosis, rheumatoid arthritis, sensation of heaviness, . FOSAMAX PLUS D dosage: unknown. During the same period patient was treated with ALTACE, METFORMIN. Patient recovered.
Rebif Side Effects Report #5757949-7
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on May 16, 2008. Female patient, 36 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: gingival bleeding, gingival disorder, injection site reaction, mouth haemorrhage, transplant, . REBIF dosage: unknown. Patient recovered.
Fosamax Side Effects Report #5706393-7
Health Professional from UNITED STATES reported FOSAMAX problem on Apr 09, 2008. Female patient, 53 years of age, was diagnosed with osteoporosis, hip fracture and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: cough, gingival disorder, gingival pain, hip fracture, lower limb fracture, osteonecrosis, wheezing, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5710389-9
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 11, 2008. Female patient, 62 years of age, was diagnosed with osteoporosis, hypothyroidism and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: diverticulitis, gingival disorder, gingival recession, oral infection, . FOSAMAX dosage: unknown. During the same period patient was treated with LEVOXYL. Patient was hospitalized. Patient recovered.
Aredia Side Effects Report #5353486-2
Consumer or non-health professional from UNITED STATES reported AREDIA problem on June 05, 2007. Female patient was diagnosed with osteoporosis and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: endodontic procedure, gingival disorder, jaw disorder, osteonecrosis, saliva altered, tooth disorder, tooth fracture, tooth loss, . AREDIA dosage: unknown. During the same period patient was treated with REMICADE. Patient recovered.
Aredia Side Effects Report #5360141-1
AREDIA problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Female patient, 47 years of age, was diagnosed with osteoporosis and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: endodontic procedure, gingival disorder, jaw disorder, osteonecrosis, saliva altered, tooth disorder, tooth fracture, tooth loss, . AREDIA dosage: unknown. During the same period patient was treated with REMICADE. Patient recovered.
Whitening Side Effects Report #5323887-7
Health Professional from UNITED STATES reported WHITENING PRE problem on May 10, 2007. Female patient, 58 years of age, weighting 150.0 lb, was diagnosed with tooth discolouration and was treated with WHITENING PRE. After drug was administered, patient experienced the following problems/side effects: dysphagia, gingival disorder, gingival pain, gingival swelling, glossodynia, nasopharyngeal disorder, pharyngeal oedema, pharyngolaryngeal pain, . WHITENING PRE dosage: unknown. Patient recovered.