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APPLICATION SITE WARMTH side effect

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Protopic Side Effects Report #5622001-8
Physician from JAPAN reported PROTOPIC problem on Jan 21, 2008. Male patient, 13 years of age, was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: application site warmth, kaposi's varicelliform eruption, . PROTOPIC dosage: unknown. During the same period patient was treated with PALDES, VOALLA, WHITE PETROLEUM, HIRUDOID, ALLEGRA, LIDOMEX, DIFLUPREDNATE, ANTEBATE. Patient was hospitalized. Patient recovered.

Abreva Side Effects Report #5462839-3
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 26, 2007. Female patient, 47 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site warmth, blister, lip swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5670790-9
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Mar 07, 2008. Female patient, weighting 142.0 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 pruritus, application site warmth, eye disorder, fatigue, hyperhidrosis, polyp, restlessness, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient recovered.

Protopic Side Effects Report #5483242-6
PROTOPIC problem was reported by a Physician from JAPAN on Sept 25, 2007. Male patient, 13 years of age, was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: application site infection, application site warmth, kaposi's varicelliform eruption, . PROTOPIC dosage: unknown. During the same period patient was treated with PALDES, VOALLA, WHITE PETROLEUM, HIRUDOID, ALLEGRA, LIDOMEX, DIFLUPREDNATE, ANTEBATE. Patient was hospitalized. Patient recovered.


Abreva Side Effects Report #5461326-6
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Sept 14, 2006. Female patient, 64 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site paraesthesia, application site warmth, . ABREVA dosage: unknown. Patient recovered.

Duragesic Side Effects Report #5341796-4
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on May 23, 2007. Female patient, weighting 180.0 lb, was diagnosed with back pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site rash, application site warmth, headache, palpitations, throat tightness, . DURAGESIC dosage: unknown. Patient recovered.

Commit Side Effects Report #5516232-5
Consumer or non-health professional from UNITED STATES reported COMMIT problem on Jan 11, 2007. Female patient, 46 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site exfoliation, application site urticaria, application site warmth, malaise, retching, . COMMIT dosage: unknown. During the same period patient was treated with NICORETTE, NICODERM CQ, NICODERM CQ. Patient recovered.

Nicotine Side Effects Report #5551203-4
NICOTINE problem was reported by a Consumer or non-health professional from UNITED STATES on July 02, 2007. Female patient, 28 years of age, weighting 201.1 lb, was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site urticaria, application site warmth, . NICOTINE dosage: 21 MG, ONCE/SINGLE, TRANSDERMAL. During the same period patient was treated with ZOLOFT. Patient recovered.

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.


Neupro Side Effects Report #5675454-3
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Female patient, 72 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 erythema, application site reaction, application site warmth, . NEUPRO dosage: 2MG/24H,1 IN 1 D,TRANSDERMAL; 6MG/24H,1 IN 1 D, TRANSDERMAL. During the same period patient was treated with ASPIRIN, LIPITOR, XALATAN, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, TRUSOPT EYEDROPS, TIMOPTIC. Patient recovered.

Bactroban Side Effects Report #5334234-9
Consumer or non-health professional from UNITED STATES reported BACTROBAN problem on Jan 24, 2007. Female patient, 93 years of age, was diagnosed with skin lesion and was treated with BACTROBAN. After drug was administered, patient experienced the following problems/side effects: application site discolouration, application site erythema, application site warmth, . BACTROBAN dosage: unknown. During the same period patient was treated with LIPITOR, TOPROL, SYNTHROID, ASPIRIN, ASCORBIC ACID. Patient recovered.