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APPLICATION SITE SWELLING side effect

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Emsam Side Effects Report #5546070-9
Health Professional from UNITED STATES reported EMSAM problem on Sept 20, 2007. Female patient, 40 years of age, was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site swelling, . EMSAM dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461320-5
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 12, 2006. Male patient, 44 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461616-7
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Nov 14, 2006. Female patient, 23 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461663-5
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 23, 2006. Female patient, 28 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.


Abreva Side Effects Report #5461732-X
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Dec 13, 2006. Female patient, 32 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461779-3
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 15, 2006. Female patient, 22 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461801-4
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Dec 19, 2006. Female patient, 20 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461977-9
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 04, 2007. Female patient, 20 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461999-8
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Apr 10, 2007. Female patient, 18 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.


Abreva Side Effects Report #5462054-3
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 19, 2007. Female patient, 38 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462090-7
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Apr 27, 2007. Female patient, 19 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462158-5
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on May 11, 2007. Female patient, 22 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, hypersensitivity, swelling face, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462201-3
Consumer or non-health professional from UNITED STATES reported ABREVA problem on May 22, 2007. Female patient, 62 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, burning sensation, hypersensitivity, oral herpes, pigmentation lip, scar, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462231-1
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on May 30, 2007. Female patient, 25 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.


Abreva Side Effects Report #5462514-5
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Jan 25, 2007. Female patient, 56 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462521-2
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 25, 2007. Female patient, 28 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462578-9
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Feb 05, 2007. Female patient, 32 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462585-6
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 06, 2007. Female patient, 46 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, swelling face, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462680-1
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Feb 22, 2007. Female patient, 46 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, lip swelling, . ABREVA dosage: unknown. Patient recovered.


Abreva Side Effects Report #5462740-5
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2007. Female patient, 32 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462824-1
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Mar 21, 2007. Female patient, 23 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, hypersensitivity, . ABREVA dosage: unknown. During the same period patient was treated with BIRTH CONTROL. Patient recovered.

Abreva Side Effects Report #5462880-0
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 02, 2007. Female patient, 54 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Neupro Side Effects Report #5676778-6
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Jan 07, 2008. Female patient was diagnosed with restless legs syndrome and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site swelling, . NEUPRO dosage: 6MG/24H, 1 IN 1. During the same period patient was treated with CYMBALTA, AMBIEN, REQUIP. Patient recovered.

Fentanyl Side Effects Report #5657084-2
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 29, 2008. Female patient, weighting 120.0 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 erythema, application site swelling, device leakage, energy increased, multiple sclerosis, pain, therapeutic response decreased, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, PERCOCET, LYRICA, CYMBALTA. Patient recovered.

Benadryl Side Effects Report #5689331-5
Consumer or non-health professional from UNITED STATES reported BENADRYL problem on Mar 20, 2008. Female patient, 16 years of age, weighting 119.0 lb, was diagnosed with rash and was treated with BENADRYL. After drug was administered, patient experienced the following problems/side effects: application site irritation, application site swelling, . BENADRYL dosage: unknown. During the same period patient was treated with BENADRYL CREAM EXTRA STRENGTH. Patient recovered.

Elidel Side Effects Report #5662017-9
ELIDEL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2007. Female patient, 13 years of age, was diagnosed with hypersensitivity and was treated with ELIDEL. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site swelling, condition aggravated, . ELIDEL dosage: unknown. Patient recovered.

Altabax Side Effects Report #5511336-5
Consumer or non-health professional from UNITED STATES reported ALTABAX problem on Sept 17, 2007. Female patient, 45 years of age, was diagnosed with staphylococcal infection and was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site inflammation, application site swelling, . ALTABAX dosage: unknown. During the same period patient was treated with BACTRIM DS. Patient recovered.

Abreva Side Effects Report #5461162-0
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 26, 2006. Female patient, 58 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462098-1
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Apr 30, 2007. Female patient, 19 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site anaesthesia, application site swelling, lip swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462122-6
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on May 03, 2007. Male patient, 60 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462338-9
Consumer or non-health professional from UNITED STATES reported ABREVA problem on July 02, 2007. Female patient, 47 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site swelling, oedema mouth, rash, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462584-4
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 06, 2007. Female patient, 24 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462804-6
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Mar 15, 2007. Female patient, 27 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site scar, application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5746056-5
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on May 13, 2008. Female patient, weighting 168.0 lb, was diagnosed with back pain, hypertension, anxiety and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site irritation, application site swelling, restless legs syndrome, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with LISINOPRIL, PROCARDIA, KLONOPIN, EPIDURALS. Patient recovered.

Neupro Side Effects Report #5676786-5
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Jan 22, 2008. Female patient, 60 years of age, weighting 175.0 lb, was diagnosed with parkinson's disease and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site reaction, application site swelling, . NEUPRO dosage: 6MG/24H, 1 IN 1 D; 4MG/24H, 1 IN 1 D; 2MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Aldara Side Effects Report #5703576-7
ALDARA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 29, 2008. Male patient, 47 years of age, was diagnosed with basal cell carcinoma and was treated with ALDARA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site swelling, arthralgia, back pain, central nervous system lesion, headache, hypertension, lymphadenopathy, . ALDARA dosage: unknown. Patient was hospitalized. Patient recovered.

Neupro Side Effects Report #5711588-2
Consumer or non-health professional from GERMANY reported NEUPRO problem on Mar 13, 2008. Female patient, 76 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 rash, application site swelling, application site vesicles, . NEUPRO dosage: 2 MG/24H (2 MG/24H 1 IN 1 DAY (S)) TRANSDERMAL, 4 MG/24H (4 MG/24H 1 IN 1 DAY (S)) TRANSDERMAL. Patient recovered.

Voltaren Side Effects Report #5255357-9
VOLTAREN problem was reported by a Physician from BRAZIL on Feb 25, 2007. Female patient, 54 years of age, weighting 160.9 lb, was diagnosed with exostosis, hypertension, diabetes mellitus non-insulin-dependent and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: anorexia, application site swelling, cerebrovascular accident, dizziness, dyspnoea, epilepsy, gait disturbance, grip strength decreased, hypoaesthesia, . VOLTAREN dosage: 125 MG/DAY. During the same period patient was treated with CAPTOPRIL, GLIBENCLAMIDE, SALICIN, GLIMEPIRIDE, DIAZEPAM. Patient was hospitalized. Patient recovered.

Exelon Side Effects Report #5672268-5
Consumer or non-health professional from UNITED STATES reported EXELON problem on Mar 14, 2008. Female patient, 82 years of age, was diagnosed with dementia and was treated with EXELON. After drug was administered, patient experienced the following problems/side effects: anorexia, application site erythema, application site swelling, chills, dyspnoea, faecal incontinence, hyperventilation, tremor, . EXELON dosage: 4.6 MG, QD. Patient was hospitalized. Patient recovered.

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.

Lubriderm Side Effects Report #5637831-6
Consumer or non-health professional from UNITED STATES reported LUBRIDERM DAILY MOISTURE problem on Feb 13, 2008. Male patient, 70 years of age, weighting 224.0 lb, was diagnosed with dry skin and was treated with LUBRIDERM DAILY MOISTURE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site swelling, application site vesicles, application site warmth, sleep disorder, . LUBRIDERM DAILY MOISTURE dosage: unknown. During the same period patient was treated with DIOVAN, ATENOLOL, ZOCOR, HYDROCHLOROTHIAZIDE. Patient recovered.

Neupro Side Effects Report #5608516-7
NEUPRO problem was reported by a Consumer or non-health professional from GERMANY on Jan 11, 2008. Female patient, 83 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 discharge, application site erythema, application site swelling, . NEUPRO dosage: unknown. Patient recovered.

Bengay Side Effects Report #5552970-6
Consumer or non-health professional from UNITED STATES reported BENGAY problem on Nov 28, 2007. Male patient, 27 years of age, weighting 145.0 lb, was diagnosed with lower limb fracture and was treated with BENGAY. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site reaction, application site swelling, peripheral coldness, poor peripheral circulation, skin discolouration, . BENGAY dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462109-3
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on May 02, 2007. Female patient, 60 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site bleeding, application site dryness, application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462237-2
Consumer or non-health professional from UNITED STATES reported ABREVA problem on June 01, 2007. Female patient, 25 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, application site scar, application site swelling, hypersensitivity, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462752-1
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2007. Female patient, 36 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site dryness, application site pain, application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Catapres Side Effects Report #5426841-X
Consumer or non-health professional from UNITED STATES reported CATAPRES problem on Oct 12, 2006. Male patient, 84 years of age, was diagnosed with tic, anxiety and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site swelling, somnolence, . CATAPRES dosage: unknown. During the same period patient was treated with PROZAC, RISPERDAL. Patient recovered.

Nicorette Side Effects Report #5388114-3
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2006. Female patient, 55 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site swelling, application site urticaria, cough, dry throat, hypersensitivity, throat irritation, . NICORETTE dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Triamcinolone Side Effects Report #5400054-X
Consumer or non-health professional from UNITED STATES reported TRIAMCINOLONE ACETONIDE problem on July 26, 2007. Female patient, 39 years of age, weighting 315.0 lb, was diagnosed with dermatitis contact, pruritus, rash pustular and was treated with TRIAMCINOLONE ACETONIDE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pustules, application site swelling, discomfort, hypersensitivity, pain of skin, pyrexia, skin burning sensation, . TRIAMCINOLONE ACETONIDE dosage: unknown. During the same period patient was treated with TRIAMCINOLONE ACETONIDE, TRIAMCINOLONE ACETONIDE, BENADRYL, PANAMA JACKS SUNBURN ALOE VERA GEL WITH LIDOCAINE. Patient recovered.

Nicorette Side Effects Report #5388114-3
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2006. Female patient, 55 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site swelling, application site urticaria, cough, dry throat, hypersensitivity, throat irritation, . NICORETTE dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Triamcinolone Side Effects Report #5400054-X
Consumer or non-health professional from UNITED STATES reported TRIAMCINOLONE ACETONIDE problem on July 26, 2007. Female patient, 39 years of age, weighting 315.0 lb, was diagnosed with dermatitis contact, pruritus, rash pustular and was treated with TRIAMCINOLONE ACETONIDE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pustules, application site swelling, discomfort, hypersensitivity, pain of skin, pyrexia, skin burning sensation, . TRIAMCINOLONE ACETONIDE dosage: unknown. During the same period patient was treated with TRIAMCINOLONE ACETONIDE, TRIAMCINOLONE ACETONIDE, BENADRYL, PANAMA JACKS SUNBURN ALOE VERA GEL WITH LIDOCAINE. Patient recovered.