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APHTHOUS STOMATITIS side effect

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Immucyst Side Effects Report #5646310-1
Health Professional from FRANCE reported IMMUCYST problem on Feb 29, 2008. Male patient, 66 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, arthralgia, conjunctivitis, penile ulceration, . IMMUCYST dosage: unknown. Patient was hospitalized. Patient recovered.

Norvasc Side Effects Report #5649663-3
NORVASC problem was reported by a Consumer or non-health professional from INDONESIA on Feb 21, 2008. Female patient, 60 years of age, was diagnosed with hypertension and was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, . NORVASC dosage: DAILY DOSE:5MG-TEXT:5 MG-FREQ:ONCE DAILY. Patient recovered.

Fosamax Side Effects Report #5654331-8
Physician from UNITED STATES reported FOSAMAX problem on Feb 25, 2008. Female patient, 86 years of age, weighting 101.4 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, barotrauma, cardiac failure congestive, cataract, cerumen impaction, chronic obstructive pulmonary disease, deafness neurosensory, gingival pain, lymphoedema, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Tyverb Side Effects Report #5656981-1
TYVERB problem was reported by a Physician from FRANCE on Mar 06, 2008. Female patient, 66 years of age, weighting 125.7 lb, was treated with TYVERB. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, pulmonary embolism, . TYVERB dosage: 1250MG PER DAY. During the same period patient was treated with XELODA. Patient was hospitalized. Patient recovered.


Aleve Side Effects Report #5658885-7
Consumer or non-health professional from UNITED STATES reported ALEVE problem on May 01, 2007. Female patient, 43 years of age, weighting 134.5 lb, was diagnosed with neck pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, lip swelling, tongue ulceration, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. During the same period patient was treated with LOESTRIN. Patient recovered.

Aleve Side Effects Report #5659776-8
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 17, 2007. Female patient, 44 years of age, weighting 200.6 lb, was diagnosed with dysmenorrhoea and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, erythema, paraesthesia oral, rash macular, skin exfoliation, skin lesion, swelling face, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. During the same period patient was treated with LOTREL, PRILOSEC. Patient recovered.

Midol Side Effects Report #5660553-2
Consumer or non-health professional from UNITED STATES reported MIDOL EXTENDED RELIEF CAPLET problem on Feb 08, 2008. Female patient, 34 years of age, weighting 145.5 lb, was treated with MIDOL EXTENDED RELIEF CAPLET. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, hypersensitivity, lip swelling, thermal burn, . MIDOL EXTENDED RELIEF CAPLET dosage: unknown. Patient recovered.

Ramipril Side Effects Report #5660880-9
RAMIPRIL problem was reported by a Physician from ESTONIA on Mar 04, 2008. Female patient, 76 years of age, weighting 138.9 lb, was diagnosed with hypertension, dyslipidaemia, coronary artery bypass and was treated with RAMIPRIL. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, colitis ulcerative, oral pain, pyrexia, vomiting, . RAMIPRIL dosage: 2.5 MG. During the same period patient was treated with NORVASC, CRESTOR, BETALOC ZOC, PLAVIX. Patient was hospitalized. Patient recovered.

Listerine Side Effects Report #5661089-5
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING PRE problem on Feb 22, 2008. Male patient, 61 years of age, weighting 152.0 lb, was diagnosed with dental care and was treated with LISTERINE WHITENING PRE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, blister, gingival bleeding, . LISTERINE WHITENING PRE dosage: unknown. During the same period patient was treated with ATENOLOL, DOXAZOSIN MESYLATE, TRIAMTHIAZID, NORVASC, ASPIRIN, LIPITOR. Patient recovered.


Seretide Side Effects Report #5661739-3
SERETIDE problem was reported by a Physician from CROATIA (local name: Hrvatska) on Mar 04, 2008. Male patient, 16 years of age, was treated with SERETIDE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, cheilitis, pyrexia, . SERETIDE dosage: unknown. Patient recovered.

Lamictal Side Effects Report #5669463-8
Physician from AUSTRIA reported LAMICTAL problem on Mar 07, 2008. Female patient, child 8 years of age, weighting 85.98 lb, was diagnosed with epilepsy and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, eyelid oedema, lip swelling, mouth ulceration, oedema mouth, rash, . LAMICTAL dosage: 25MG PER DAY. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5677793-9
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 14, 2008. Female patient, 35 years of age, weighting 154.3 lb, was diagnosed with resorption bone increased, osteoporosis, diabetes mellitus and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, exostosis, hypersensitivity, internal fixation of fracture, lip swelling, lower limb deformity, osteoarthritis, temporomandibular joint syndrome, upper respiratory tract infection, . FOSAMAX dosage: unknown. During the same period patient was treated with GLYBURIDE, METFORMIN, PREMARIN. Patient was hospitalized. Patient recovered.

Listerine Side Effects Report #5677858-1
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING QUICK DISSOLVING STRIPS problem on Mar 11, 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: aphthous stomatitis, burning sensation, infection, insomnia, lip ulceration, mouth haemorrhage, oral discomfort, pain, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. Patient recovered.

Immucyst Side Effects Report #5682160-8
IMMUCYST problem was reported by a Health Professional from FRANCE on Mar 21, 2008. Male patient, 66 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, arthralgia, conjunctivitis, penile ulceration, . IMMUCYST dosage: unknown. Patient was hospitalized. Patient recovered.


Orencia Side Effects Report #5682638-7
Physician from UNITED STATES reported ORENCIA problem on Jan 22, 2008. Female patient, 69 years of age, was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, . ORENCIA dosage: unknown. Patient recovered.

Fosamax Side Effects Report #5622501-0
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 01, 2008. Female patient, 86 years of age, weighting 101.4 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, cardiac failure congestive, cataract, chronic obstructive pulmonary disease, gingival pain, lymphoedema, neurodermatitis, osteomyelitis, osteonecrosis, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Listerine Side Effects Report #5622881-6
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING QUICK DISSOLVING STRIPS problem on Jan 25, 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: aphthous stomatitis, insomnia, mouth haemorrhage, mouth injury, oral infection, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. Patient recovered.

Januvia Side Effects Report #5629760-9
JANUVIA problem was reported by a Health Professional from UNITED STATES on Feb 11, 2008. Female patient, 47 years of age, weighting 222.7 lb, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, diarrhoea, pancreatitis, urticaria, . JANUVIA dosage: unknown. During the same period patient was treated with BYETTA, GLUCOPHAGE, TRICOR, TORSEMIDE, CRESTOR, DIOVAN, PAXIL, LANTUS. Patient was hospitalized and became disabled. Patient recovered.

Januvia Side Effects Report #5633281-7
Health Professional from UNITED STATES reported JANUVIA problem on Feb 11, 2008. Female patient, 47 years of age, weighting 222.7 lb, was diagnosed with type 2 diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, diarrhoea, pancreatitis, urticaria, . JANUVIA dosage: unknown. During the same period patient was treated with BYETTA, GLUCOPHAGE, TRICOR, TORSEMIDE, CRESTOR, DIOVAN, PAXIL, LANTUS. Patient was hospitalized and became disabled. Patient recovered.


Prograf Side Effects Report #5633426-9
PROGRAF problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 07, 2008. Male patient, 62 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, bacterial infection, bundle branch block right, culture urine positive, hypotension, myocardial infarction, nephritis interstitial, neutropenia, . PROGRAF dosage: 4 MG, BID, ORAL; 1.5 MG, BID, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, PREDNISONE, METHYLPREDNISOLONE, THYMOGLOBULIN, DAPSONE. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5638916-0
Pharmacist from UNITED STATES reported CHANTIX problem on Feb 25, 2008. Female patient, 59 years of age, weighting 170.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, depression, mental status changes, nicotine dependence, withdrawal syndrome, . CHANTIX dosage: unknown. Patient recovered.

Byetta Side Effects Report #5639288-8
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 18, 2008. Male patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, blood glucose increased, complication of device insertion, dry mouth, hospitalisation, wound infection staphylococcal, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, GLYBURIDE. Patient was hospitalized. Patient recovered.

Nicorette Side Effects Report #5641130-6
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on Jan 29, 2007. Female patient, 54 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, pharyngolaryngeal pain, throat irritation, . NICORETTE dosage: unknown. Patient recovered.

Nicorette Side Effects Report #5641472-4
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2007. Male patient, 52 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, oral pain, . NICORETTE dosage: unknown. Patient recovered.

Nicorette Side Effects Report #5641587-0
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on Nov 19, 2007. Female patient, 78 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, oral discomfort, oral mucosal eruption, oral pain, . NICORETTE dosage: unknown. Patient recovered.

Valtrex Side Effects Report #5581943-2
VALTREX problem was reported by a Physician from JAPAN on Dec 28, 2007. Male patient, 67 years of age, weighting 132.3 lb, was diagnosed with herpes zoster, pruritus, central pain syndrome, lipids abnormal and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, eating disorder, haematuria, hydronephrosis, pyrexia, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with ALLELOCK, CELESTAMINE, FLUVOXAMINE MALEATE, TEGRETOL, SIMVASTATIN, ZOVIRAX. Patient recovered.

Chantix Side Effects Report #5590715-4
Physician from PORTUGAL reported CHANTIX problem on Jan 02, 2008. Female patient, weighting 119.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, lip oedema, viral infection, . CHANTIX dosage: unknown. During the same period patient was treated with BELARA. Patient recovered.

Byetta Side Effects Report #5600645-7
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Male patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, blood glucose increased, complication of device insertion, dry mouth, hospitalisation, wound infection staphylococcal, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, GLYBURIDE. Patient was hospitalized. Patient recovered.

Proair Side Effects Report #5601193-0
Consumer or non-health professional from UNITED STATES reported PROAIR HFA problem on Jan 22, 2008. Female patient, 36 years of age, weighting 250.0 lb, was diagnosed with asthma and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, cheilitis, erythema, gingival swelling, gingivitis, . PROAIR HFA dosage: unknown. Patient recovered.

Chantix Side Effects Report #5603229-X
CHANTIX problem was reported by a Physician from PORTUGAL on Jan 14, 2008. Female patient, weighting 119.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, lip oedema, viral infection, . CHANTIX dosage: unknown. During the same period patient was treated with BELARA. Patient recovered.

Cymbalta Side Effects Report #5604630-0
Consumer or non-health professional from UNITED STATES reported CYMBALTA problem on Jan 24, 2008. Female patient, 55 years of age, weighting 247.0 lb, was diagnosed with affective disorder and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, lip ulceration, tongue ulceration, . CYMBALTA dosage: 10MG DAILY PO. Patient recovered.

Prograf Side Effects Report #5605137-7
PROGRAF problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2008. Male patient, 62 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, bundle branch block right, hypotension, infection, kidney transplant rejection, myocardial infarction, nephritis interstitial, neutropenia, tachycardia, . PROGRAF dosage: 4 MG, BID, ORAL; 1.5 MG, BID, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, MYCOPHENOLATE MOFETIL, PREDNISONE, METHYLPREDNISOLONE, THYMOGLOBULIN, DAPSONE. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5536934-4
Physician from FINLAND reported ZOMETA problem on Nov 30, 2007. Female patient was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, osteonecrosis, . ZOMETA dosage: 4MG, TWICE A YEAR. Patient recovered.

Valtrex Side Effects Report #5537398-7
VALTREX problem was reported by a Physician from JAPAN on Nov 30, 2007. Male patient, 67 years of age, weighting 132.3 lb, was diagnosed with herpes zoster, pruritus, central pain syndrome, lipids abnormal and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, eating disorder, haematuria, hydronephrosis, pyrexia, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with ALLELOCK, CELESTAMINE, FLUVOXAMINE MALEATE, TEGRETOL, SIMVASTATIN, ZOVIRAX. Patient recovered.

Caelyx Side Effects Report #5553911-8
Physician from SPAIN reported CAELYX problem on Dec 05, 2007. Female patient, 54 years of age, was diagnosed with ovarian cancer and was treated with CAELYX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, erythema, skin exfoliation, skin lesion, skin reaction, stevens-johnson syndrome, swelling, swollen tongue, toxic skin eruption, . CAELYX dosage: unknown. Patient was hospitalized. Patient recovered.

Listerine Side Effects Report #5556217-6
LISTERINE WHITENING PRE problem was reported by a Consumer or non-health professional from CANADA on Nov 27, 2007. Female patient was treated with LISTERINE WHITENING PRE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, burning sensation, gingival swelling, rash pustular, . LISTERINE WHITENING PRE dosage: unknown. Patient recovered.

Humira Side Effects Report #5560016-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Oct 27, 2007. Female patient, weighting 93.08 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, . HUMIRA dosage: unknown. Patient recovered.

Cool Side Effects Report #5564155-8
COOL CITRUS LISTERINE MOUTHWASH problem was reported by a Consumer or non-health professional from BRAZIL on Dec 04, 2007. Male patient, 26 years of age, weighting 180.8 lb, was diagnosed with dental disorder prophylaxis and was treated with COOL CITRUS LISTERINE MOUTHWASH. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, oral disorder, oral pain, speech disorder, . COOL CITRUS LISTERINE MOUTHWASH dosage: 10 ML BID (10 ML), ORAL. Patient recovered.

Pravachol Side Effects Report #5566986-7
Consumer or non-health professional from UNITED STATES reported PRAVACHOL problem on Aug 22, 2007. Female patient, 60 years of age, weighting 200.6 lb, was diagnosed with blood cholesterol increased and was treated with PRAVACHOL. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, paraesthesia oral, . PRAVACHOL dosage: unknown. During the same period patient was treated with WELLBUTRIN, PROZAC. Patient recovered.

Caelyx Side Effects Report #5569406-1
CAELYX problem was reported by a Physician from SPAIN on Dec 17, 2007. Female patient, 54 years of age, was diagnosed with ovarian cancer and was treated with CAELYX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, erythema, skin exfoliation, skin lesion, skin reaction, stevens-johnson syndrome, swelling, swollen tongue, toxic skin eruption, . CAELYX dosage: unknown. During the same period patient was treated with VITAMIN B6. Patient was hospitalized. Patient recovered.

Ticlid Side Effects Report #5574635-7
Physician from FRANCE reported TICLID problem on Dec 17, 2007. Male patient, 50 years of age, was diagnosed with angioplasty and was treated with TICLID. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, neutropenia, . TICLID dosage: unknown. Patient recovered.

Chantix Side Effects Report #5575123-4
CHANTIX problem was reported by a Physician from PORTUGAL on Dec 18, 2007. Female patient, weighting 130.1 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, glossitis, tongue oedema, . CHANTIX dosage: unknown. Patient recovered.

Chantix Side Effects Report #5578230-5
Consumer or non-health professional from PORTUGAL reported CHANTIX problem on Dec 19, 2007. Female patient, weighting 165.3 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, astigmatism, cellulitis, chronic sinusitis, eye disorder, headache, menorrhagia, myopia, . CHANTIX dosage: unknown. During the same period patient was treated with FLUOXETINE, CASTILIUM. Patient recovered.

Orencia Side Effects Report #5507431-7
ORENCIA problem was reported by a Physician from GERMANY on Nov 02, 2007. Female patient, 45 years of age, weighting 154.3 lb, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, leukopenia, neutropenia, . ORENCIA dosage: DOSE 750 MG ON 01-OCT-2007 AND 31-OCT-2007.. During the same period patient was treated with METHOTREXATE. Patient recovered.

Prezista Side Effects Report #5512331-2
Health Professional from FRANCE reported PREZISTA problem on Nov 02, 2007. Male patient, 43 years of age, was diagnosed with hiv infection, infection prophylaxis and was treated with PREZISTA. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, pyrexia, . PREZISTA dosage: unknown. During the same period patient was treated with SULFAMETHOXAZOLE AND TRIMETHOPRIM, RITONAVIR, EMTRICITABINE, LOPINAVIR AND RITONAVIR. Patient was hospitalized. Patient recovered.

Commit Side Effects Report #5516029-6
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 17, 2006. Female patient, 73 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, nicotine dependence, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ, NICODERM CQ, NICODERM CQ. Patient recovered.

Commit Side Effects Report #5516114-9
Consumer or non-health professional from UNITED STATES reported COMMIT problem on Dec 15, 2006. Female patient, 79 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, . COMMIT dosage: unknown. Patient recovered.

Commit Side Effects Report #5516190-3
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 05, 2007. Male patient, 23 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, oral discomfort, . COMMIT dosage: unknown. Patient recovered.

Commit Side Effects Report #5516990-X
Consumer or non-health professional from UNITED STATES reported COMMIT problem on June 26, 2007. Female patient, 69 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, oral fungal infection, oral pain, . COMMIT dosage: unknown. Patient recovered.

Commit Side Effects Report #5517184-4
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 24, 2007. Female patient, 42 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, . COMMIT dosage: unknown. Patient recovered.

Listerine Side Effects Report #5519195-1
Consumer or non-health professional from CANADA reported LISTERINE WHITENING PRE problem on Nov 05, 2007. Female patient was treated with LISTERINE WHITENING PRE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, burning sensation, gingival oedema, rash pustular, . LISTERINE WHITENING PRE dosage: unknown. Patient recovered.