APPLICATION SITE BURN side effect
What is APPLICATION SITE BURN ?Drugs associated with APPLICATION SITE BURN
ABREVA ALTABAX BENGAY BUCKLEY CAPZASIN CATAPRES DESITIN DURAGESIC EQUATE FENTANYL FINACEA LISTERINE MONISTAT NEUPRO NEURONTIN NICORETTE NICOTINE PAIN SUDACARE TIGER VISINEAPPLICATION SITE BURN : Monistat Side Effects Report #5654695-5
Consumer or non-health professional from UNITED STATES reported MONISTAT problem on Feb 28, 2008. Female patient, weighting 138.0 lb, was diagnosed with fungal infection and was treated with MONISTAT. After drug was administered, patient experienced the following problems/side effects: application site burn, vulvovaginal burning sensation, vulvovaginal discomfort, vulvovaginal dryness, . MONISTAT dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Desitin Side Effects Report #5668110-9
DESITIN DIAPER RASH problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 03, 2008. Female patient was diagnosed with dermatitis diaper and was treated with DESITIN DIAPER RASH. After drug was administered, patient experienced the following problems/side effects: application site burn, pain, . DESITIN DIAPER RASH dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Bengay Side Effects Report #5672428-3
Consumer or non-health professional from UNITED STATES reported BENGAY PAIN RELIEVING PATCH problem on Mar 11, 2008. Male patient, 27 years of age, weighting 170.0 lb, was diagnosed with pain in extremity and was treated with BENGAY PAIN RELIEVING PATCH. After drug was administered, patient experienced the following problems/side effects: application site burn, burns second degree, scab, . BENGAY PAIN RELIEVING PATCH dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Bengay Side Effects Report #5675764-X
BENGAY ULTRA STRENGTH PATCH problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Female patient, 84 years of age, weighting 165.0 lb, was diagnosed with pain and was treated with BENGAY ULTRA STRENGTH PATCH. After drug was administered, patient experienced the following problems/side effects: application site burn, . BENGAY ULTRA STRENGTH PATCH dosage: unknown. During the same period patient was treated with COUMDAIN. Patient recovered.
APPLICATION SITE BURN : Altabax Side Effects Report #5684465-3
Health Professional from UNITED STATES reported ALTABAX problem on Mar 27, 2008. Female patient, 66 years of age, weighting 117.0 lb, was diagnosed with skin irritation and was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site burn, application site pain, . ALTABAX dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Neupro Side Effects Report #5691299-2
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 18, 2008. Male patient, 55 years of age, was diagnosed with parkinson's disease and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site burn, application site erythema, application site swelling, . NEUPRO dosage: 2MG/24H,1 IN 1 D,TRANSDERMAL; 4MG/24H,1 IN 1 D,TRANSDERMAL ; 6MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with SINEMET, AMANTADINE, PROZAC, FLOMAX. Patient recovered.
APPLICATION SITE BURN : Nicorette Side Effects Report #5625496-9
Consumer or non-health professional from UNITED KINGDOM reported NICORETTE problem on Jan 30, 2008. Female patient, 39 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site burn, application site irritation, application site pain, discomfort, scab, . NICORETTE dosage: 10 MG PATCH ONCE (10 MG), TOPICAL. Patient recovered.
APPLICATION SITE BURN : Pain Side Effects Report #5627198-1
PAIN PATCH BACK ASPERCREME problem was reported by a Health Professional from UNITED STATES on Feb 12, 2008. Female patient, weighting 170.0 lb, was diagnosed with back pain and was treated with PAIN PATCH BACK ASPERCREME. After drug was administered, patient experienced the following problems/side effects: application site burn, application site vesicles, pain, . PAIN PATCH BACK ASPERCREME dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Listerine Side Effects Report #5630644-0
Consumer or non-health professional from UNITED STATES reported LISTERINE WHITENING QUICK DISSOLVING STRIPS problem on Feb 04, 2008. Female patient, 73 years of age, 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: application site burn, gingivitis, . LISTERINE WHITENING QUICK DISSOLVING STRIPS dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN C, ACETAMINOPHEN, FISH OIL, CENTRUM, ASPIRIN. Patient recovered.
APPLICATION SITE BURN : Finacea Side Effects Report #5632859-4
FINACEA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 04, 2007. Female patient was diagnosed with rosacea and was treated with FINACEA. After drug was administered, patient experienced the following problems/side effects: application site burn, paraesthesia, . FINACEA dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Nicorette Side Effects Report #5636527-4
Consumer or non-health professional from AUSTRALIA reported NICORETTE problem on Feb 05, 2008. Female patient, 30 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site burn, application site erythema, application site vesicles, . NICORETTE dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Tiger Side Effects Report #5638428-4
TIGER BALM ULTRA STRENGTH HAW PAR CORPORATION LTD problem was reported by a Physician from UNITED STATES on Feb 21, 2008. Female patient was diagnosed with analgesia and was treated with TIGER BALM ULTRA STRENGTH HAW PAR CORPORATION LTD. After drug was administered, patient experienced the following problems/side effects: application site burn, application site pain, application site vesicles, dermatitis contact, . TIGER BALM ULTRA STRENGTH HAW PAR CORPORATION LTD dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Bengay Side Effects Report #5590674-4
Consumer or non-health professional from UNITED STATES reported BENGAY PAIN RELIEVING PATCH problem on Jan 02, 2008. Male patient, 27 years of age, weighting 170.0 lb, was diagnosed with pain in extremity and was treated with BENGAY PAIN RELIEVING PATCH. After drug was administered, patient experienced the following problems/side effects: application site burn, application site scab, application site vesicles, burns second degree, . BENGAY PAIN RELIEVING PATCH dosage: unknown. Patient was hospitalized. Patient recovered.
APPLICATION SITE BURN : Bengay Side Effects Report #5592804-7
BENGAY PAIN RELIEVING PATCH problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 08, 2008. Male patient was treated with BENGAY PAIN RELIEVING PATCH. After drug was administered, patient experienced the following problems/side effects: application site burn, . BENGAY PAIN RELIEVING PATCH dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Visine Side Effects Report #5553092-0
Consumer or non-health professional from UNITED STATES reported VISINE EYE DROPS problem on Nov 27, 2007. Female patient, 77 years of age, weighting 134.0 lb, was diagnosed with dry eye and was treated with VISINE EYE DROPS. After drug was administered, patient experienced the following problems/side effects: application site burn, eye irritation, ocular hyperaemia, visual disturbance, . VISINE EYE DROPS dosage: unknown. During the same period patient was treated with VERAPAMIL, MECLICINE, PLAVIX. Patient recovered.
APPLICATION SITE BURN : Catapres Side Effects Report #5555904-3
CATAPRES problem was reported by a Health Professional from UNITED STATES on Nov 19, 2007. Female patient was diagnosed with hot flush and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site burn, . CATAPRES dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Fentanyl Side Effects Report #5574404-8
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Dec 17, 2007. Female patient, weighting 125.0 lb, was diagnosed with pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site burn, application site pruritus, application site rash, blood potassium decreased, decreased appetite, dehydration, diarrhoea, therapeutic response decreased, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient was hospitalized. Patient recovered.
APPLICATION SITE BURN : Buckley Side Effects Report #5580167-2
BUCKLEY problem was reported by a Consumer or non-health professional from CANADA on Dec 14, 2007. Female patient was diagnosed with upper respiratory tract congestion and was treated with BUCKLEY. After drug was administered, patient experienced the following problems/side effects: application site burn, blister, chemical burn of skin, . BUCKLEY dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Neupro Side Effects Report #5588818-3
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Nov 06, 2007. Female patient was diagnosed with parkinson's disease and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site burn, overdose, . NEUPRO dosage: 2MG/24H,1 IN 1 D,TRANSDERMAL ; 6MG/24H,1 IN 1 D,TRANSDERMAL ; 12MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with PARCOPA, AZILECT. Patient recovered.
APPLICATION SITE BURN : Catapres Side Effects Report #5508314-9
CATAPRES problem was reported by a Pharmacist from UNITED STATES on Oct 12, 2007. Male patient, 57 years of age, was diagnosed with hypertension and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site burn, . CATAPRES dosage: unknown. During the same period patient was treated with LOTREL, DIOVAN HCT. Patient recovered.
APPLICATION SITE BURN : Nicotine Side Effects Report #5515218-4
Consumer or non-health professional from UNITED STATES reported NICOTINE problem on Nov 02, 2007. Male patient was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: application site burn, application site scar, blood pressure increased, headache, insomnia, . NICOTINE dosage: 21 MG, QD, TRANSDERMAL. Patient recovered.
APPLICATION SITE BURN : Nicorette Side Effects Report #5524814-X
NICORETTE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 08, 2007. Female patient was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site burn, application site irritation, discomfort, pain, . NICORETTE dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Catapres Side Effects Report #5475117-3
Pharmacist from UNITED STATES reported CATAPRES problem on Sept 20, 2007. Male patient, weighting 242.5 lb, was diagnosed with hypertension and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site burn, application site discharge, application site erythema, rash, . CATAPRES dosage: unknown. During the same period patient was treated with TOPROL, FELODIPINE ER, CLONIDINE, AGGRENOX, SIMVASTATIN, PLENDIL, DYAZIDE. Patient recovered.
APPLICATION SITE BURN : Catapres Side Effects Report #5479901-1
CATAPRES problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 24, 2007. Female patient was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site burn, application site erythema, . CATAPRES dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Bengay Side Effects Report #5493878-4
Consumer or non-health professional from UNITED STATES reported BENGAY problem on Oct 11, 2007. Male patient, 44 years of age, weighting 149.9 lb, was diagnosed with musculoskeletal stiffness and was treated with BENGAY. After drug was administered, patient experienced the following problems/side effects: application site burn, . BENGAY dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Bengay Side Effects Report #5495403-0
BENGAY ULTRA STRENGTH PATCH problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 17, 2007. Female patient, 36 years of age, was diagnosed with back pain and was treated with BENGAY ULTRA STRENGTH PATCH. After drug was administered, patient experienced the following problems/side effects: application site burn, application site discolouration, application site irritation, application site pruritus, . BENGAY ULTRA STRENGTH PATCH dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Equate Side Effects Report #5450055-0
Consumer or non-health professional from UNITED STATES reported EQUATE NTS problem on Sept 11, 2007. Female patient, 54 years of age, was treated with EQUATE NTS. After drug was administered, patient experienced the following problems/side effects: application site burn, application site erythema, application site pruritus, application site rash, application site reaction, application site swelling, cardiac failure congestive, depressed level of consciousness, . EQUATE NTS dosage: unknown. During the same period patient was treated with IMITREX, ANTIBIOTICS, MORPHINE. Patient was hospitalized. Patient recovered.
APPLICATION SITE BURN : Abreva Side Effects Report #5461540-X
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 01, 2006. Female patient was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site burn, . ABREVA dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Abreva Side Effects Report #5461852-X
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Dec 29, 2006. Female patient, 26 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site burn, . ABREVA dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Capzasin Side Effects Report #5469249-3
CAPZASIN HP problem was reported by a Pharmacist from UNITED STATES on Sept 25, 2007. Male patient, 37 years of age, weighting 155.0 lb, was diagnosed with myalgia and was treated with CAPZASIN HP. After drug was administered, patient experienced the following problems/side effects: application site burn, burning sensation, burns first degree, erythema, hyperaesthesia, pain, sunburn, . CAPZASIN HP dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Capzasin Side Effects Report #5470530-2
Consumer or non-health professional from UNITED STATES reported CAPZASIN problem on Sept 27, 2007. Female patient, 46 years of age, weighting 124.0 lb, was diagnosed with arthritis and was treated with CAPZASIN. After drug was administered, patient experienced the following problems/side effects: application site burn, application site irritation, application site warmth, gait disturbance, . CAPZASIN dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Bengay Side Effects Report #5474183-9
BENGAY PAIN RELIEVING PATCH problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 24, 2007. Female patient, 37 years of age, weighting 200.0 lb, was diagnosed with analgesia and was treated with BENGAY PAIN RELIEVING PATCH. After drug was administered, patient experienced the following problems/side effects: application site burn, . BENGAY PAIN RELIEVING PATCH dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Duragesic Side Effects Report #5429450-1
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Aug 20, 2007. Female patient, weighting 168.0 lb, was diagnosed with pain, rheumatoid arthritis, immune system disorder, migraine, sleep disorder, nausea and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site burn, chronic obstructive pulmonary disease, nasopharyngitis, pneumonia, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, ENBREL, METHOTREXATE, IMITREX, AMBIEN, ZOFRAN, PERCOCET. Patient was hospitalized. Patient recovered.
APPLICATION SITE BURN : Neurontin Side Effects Report #5655980-3
NEURONTIN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, weighting 160.3 lb, was diagnosed with pain, impaired gastric emptying, abdominal pain and was treated with NEURONTIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain, application site burn, application site vesicles, depression, impaired gastric emptying, mood altered, . NEURONTIN dosage: unknown. During the same period patient was treated with FENTANYL, PERCOCET. Patient was hospitalized. Patient recovered.
APPLICATION SITE BURN : Fentanyl Side Effects Report #5624320-8
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 06, 2008. Male patient, 55 years of age, weighting 250.0 lb, was diagnosed with intervertebral disc disorder and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: accidental exposure, application site burn, application site rash, eye inflammation, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM. Patient recovered.
APPLICATION SITE BURN : Duragesic Side Effects Report #5578674-1
DURAGESIC problem was reported by a Pharmacist from FRANCE on Dec 21, 2007. Female patient, 50 years of age, was diagnosed with cancer pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: anxiety, application site burn, application site irritation, pain, wound haemorrhage, . DURAGESIC dosage: unknown. During the same period patient was treated with ACTISKENAN. Patient recovered.
APPLICATION SITE BURN : Sudacare Side Effects Report #5604529-X
Consumer or non-health professional from UNITED STATES reported SUDACARE SHOWER SOOTHERS problem on Jan 14, 2008. Female patient, 15 years of age, was treated with SUDACARE SHOWER SOOTHERS. After drug was administered, patient experienced the following problems/side effects: accidental exposure, application site burn, . SUDACARE SHOWER SOOTHERS dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Duragesic Side Effects Report #5564800-7
DURAGESIC problem was reported by a Pharmacist from FRANCE on Dec 11, 2007. Female patient, 50 years of age, was diagnosed with cancer pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: anxiety, application site burn, application site irritation, pain, wound haemorrhage, . DURAGESIC dosage: unknown. During the same period patient was treated with ACTISKENAN. Patient recovered.
APPLICATION SITE BURN : Abreva Side Effects Report #5461212-1
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Aug 15, 2006. Female patient, 35 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site bleeding, application site burn, application site erythema, application site irritation, application site pruritus, application site scab, lip blister, . ABREVA dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Abreva Side Effects Report #5462362-6
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, 34 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site bleeding, application site burn, application site erythema, application site irritation, application site pain, chapped lips, oral herpes, . ABREVA dosage: unknown. Patient recovered.
APPLICATION SITE BURN : Abreva Side Effects Report #5462703-X
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Feb 26, 2007. Female patient, 30 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site bleeding, application site burn, application site discolouration, application site dryness, application site pain, application site vesicles, . ABREVA dosage: unknown. Patient recovered.