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APPLICATION SITE URTICARIA side effect

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Estradiol Side Effects Report #5616348-9
Health Professional from UNITED STATES reported ESTRADIOL problem on Feb 05, 2008. Female patient, 42 years of age, weighting 162.0 lb, was diagnosed with hot flush, menopause and was treated with ESTRADIOL. After drug was administered, patient experienced the following problems/side effects: application site urticaria, . ESTRADIOL dosage: unknown. Patient recovered.

Nicorette Side Effects Report #5641511-0
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 10, 2007. Female patient, 49 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site urticaria, hypersensitivity, mouth ulceration, paraesthesia oral, stomatitis, . NICORETTE dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Neuro Side Effects Report #5647960-9
Consumer or non-health professional from UNITED STATES reported NEURO problem on Feb 13, 2008. Male patient, 69 years of age, weighting 185.0 lb, was diagnosed with parkinson's disease and was treated with NEURO. After drug was administered, patient experienced the following problems/side effects: application site urticaria, pruritus, rash, . NEURO dosage: 6MG/24H, 1 IN 1 D, TRANSDERMAL; 4MG/2H, 1 IN 1 D, TRANSDERMAL; 2MG/24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with ARTANE, AZILECT, LIPITOR, ACTONEL. Patient recovered.

Daytrana Side Effects Report #5409463-6
DAYTRANA problem was reported by a Health Professional from UNITED STATES on July 23, 2007. Female patient, 13 years of age, weighting 175.0 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with DAYTRANA. After drug was administered, patient experienced the following problems/side effects: application site urticaria, hyperhidrosis, loss of consciousness, . DAYTRANA dosage: unknown. During the same period patient was treated with TRILEPTAL, PEPCID, ALBUTEROL, STRATTERA, SEROQUEL. Patient recovered.


Nicorette Side Effects Report #5388101-5
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on Nov 17, 2006. Female patient, 44 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site urticaria, dysgeusia, euphoric mood, ill-defined disorder, oral disorder, psychomotor hyperactivity, thinking abnormal, . NICORETTE dosage: unknown. Patient recovered.

Nicorette Side Effects Report #5388101-5
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 17, 2006. Female patient, 44 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site urticaria, dysgeusia, euphoric mood, ill-defined disorder, oral disorder, psychomotor hyperactivity, thinking abnormal, . NICORETTE dosage: unknown. Patient recovered.

Duragesic Side Effects Report #5779921-3
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on June 11, 2008. Female patient, weighting 215.0 lb, was diagnosed with back pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site urticaria, hyperhidrosis, . DURAGESIC dosage: unknown. Patient recovered.

Catapres Side Effects Report #5725652-5
CATAPRES problem was reported by a Pharmacist from UNITED STATES on Apr 04, 2008. Male patient, 68 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 urticaria, . CATAPRES dosage: unknown. During the same period patient was treated with RANITIDINE, PERCOCET, PROMETHAZINE, AVODART, TRANSDERM SCOP, FLOMAX, LORAZEPAM. Patient recovered.

Climara Side Effects Report #5698582-5
Consumer or non-health professional from UNITED STATES reported CLIMARA problem on Oct 02, 2006. Female patient, 51 years of age, weighting 149.9 lb, was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site urticaria, . CLIMARA dosage: unknown. Patient recovered.


Climara Side Effects Report #5616498-7
CLIMARA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 07, 2008. Female patient, 60 years of age, weighting 141.1 lb, was diagnosed with menopausal symptoms and was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site urticaria, . CLIMARA dosage: unknown. During the same period patient was treated with BENICAR. Patient recovered.

Neupro Side Effects Report #5618401-2
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Jan 18, 2008. Female patient, 74 years of age, weighting 130.0 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 pruritus, application site urticaria, dizziness, fall, hypotension, musculoskeletal chest pain, . NEUPRO dosage: 2MG/24H, 1 IN 1 D, TRANSDERMAL; 4MG/24H, 1 IN 1 D, TRANSDERMAL; 6 MG/24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with FLORINEF, SINEMET, FOSAMAX. Patient recovered.

Catapres Side Effects Report #5567252-6
CATAPRES problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 18, 2007. Female patient, 81 years of age, was diagnosed with hypertension, blood pressure, gastric disorder and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site discharge, application site urticaria, . CATAPRES dosage: unknown. During the same period patient was treated with ASPIRIN, PLAVIX. 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.

Commit Side Effects Report #5517257-6
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 19, 2007. Female patient, 49 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site urticaria, hypersensitivity, pharyngeal oedema, sensation of foreign body, throat tightness, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.


Commit Side Effects Report #5517307-7
Consumer or non-health professional from UNITED STATES reported COMMIT problem on Oct 11, 2007. Female patient, 52 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site pain, application site urticaria, application site vesicles, cheilitis, swollen tongue, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Catapres Side Effects Report #5531115-2
CATAPRES problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Female patient, 81 years of age, was diagnosed with hypertension, blood pressure, gastric disorder and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site discharge, application site urticaria, . CATAPRES dosage: unknown. During the same period patient was treated with ASPIRIN, PLAVIX. Patient recovered.

Nicotine Side Effects Report #5551203-4
Consumer or non-health professional from UNITED STATES reported NICOTINE problem 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.

Duragesic Side Effects Report #5428920-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient, weighting 105.0 lb, was diagnosed with pain, systemic lupus erythematosus, thyroid disorder, nervousness and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site rash, application site urticaria, menstrual disorder, . DURAGESIC dosage: unknown. During the same period patient was treated with PLAQUENIL, SYNTHROID, VALIUM, OXYCODONE. Patient recovered.

Neupro Side Effects Report #5766004-1
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on May 01, 2008. Male patient, 59 years of age, weighting 210.0 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 urticaria, balance disorder, dizziness, hyperhidrosis, palpitations, . 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, REQUIP, APOKYNECTION, LOVASTATIN, SYNTHROID. Patient recovered.


Neupro Side Effects Report #5676504-0
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 12, 2007. Male patient, 72 years of age, weighting 190.0 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 pruritus, application site urticaria, . NEUPRO dosage: 6MG/24H,1 IN 1 D,TRANSDERMAL; 2MG/24H,1 IN 1D, TRANSDERMAL. During the same period patient was treated with AZILECT, SINEMET. Patient recovered.

Neupro Side Effects Report #5676852-4
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Feb 07, 2008. Male patient, 59 years of age, weighting 210.0 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 urticaria, balance disorder, dizziness, hyperhidrosis, palpitations, . NEUPRO dosage: 2MG/24H, 1 IN 1 D, TRANSDERMAL; 4MGW/24H, 1 IN 1 D, TRANSDERMAL; 6MG/24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with SINEMET, AMANTADINE, REQUIP, APOKYNECTION, LOVASTATIN, SYNTHROID. Patient recovered.

Fentanyl Side Effects Report #5700468-4
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 01, 2008. Female patient, weighting 137.0 lb, was diagnosed with abdominal pain upper, pulmonary hypertension, sleep disorder, breakthrough pain, colitis and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site urticaria, intestinal obstruction, nail discolouration, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with XANAX, ATIVAN, PERCOCET, BENTYL. Patient recovered.

Fentanyl Side Effects Report #5712739-6
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Apr 21, 2008. Male patient, 44 years of age, weighting 185.0 lb, was diagnosed with facet joint syndrome and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site irritation, application site urticaria, skin burning sensation, skin irritation, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM. Patient recovered.

Daytrana Side Effects Report #5345547-9
DAYTRANA problem was reported by a Pharmacist from UNITED STATES on June 01, 2007. Male patient, child 8 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with DAYTRANA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site urticaria, . DAYTRANA dosage: unknown. Patient recovered.

Nicorette Side Effects Report #5260037-X
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on Feb 14, 2006. Female patient, 61 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site urticaria, hypersensitivity, rash macular, . NICORETTE dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Nicoderm Side Effects Report #5670386-9
NICODERM CQ problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 14, 2008. Female patient, 61 years of age, weighting 142.0 lb, was treated with NICODERM CQ. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, application site urticaria, . NICODERM CQ dosage: unknown. Patient recovered.

Neupro Side Effects Report #5610371-6
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Jan 09, 2008. Female patient, 81 years of age, was diagnosed with restless legs syndrome and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site urticaria, . NEUPRO dosage: 2MG/24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with GABAPENTIN, SINEMET. Patient recovered.

Nicorette Side Effects Report #5388274-4
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2007. Female patient, 79 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site rash, application site urticaria, dysphonia, . NICORETTE dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Nicorette Side Effects Report #5388274-4
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on Mar 12, 2007. Female patient, 79 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site rash, application site urticaria, dysphonia, . NICORETTE dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Exelon Side Effects Report #5735367-5
EXELON problem was reported by a Physician from UNITED STATES on Mar 27, 2008. Female patient, 64 years of age, weighting 209.9 lb, was diagnosed with dementia alzheimer's type and was treated with EXELON. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site rash, application site urticaria, . EXELON dosage: 9.5 MG, QD, TRANSDERMAL. Patient recovered.

Neupro Side Effects Report #5736056-3
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Apr 23, 2008. Female patient, 44 years of age, weighting 202.0 lb, was diagnosed with restless legs syndrome and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site urticaria, gambling, . NEUPRO dosage: 4MG/24H, 1 IN 1 D, TRANSDERMAL; 2MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Neupro Side Effects Report #5695461-4
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 18, 2008. Female patient, weighting 164.0 lb, was diagnosed with restless legs syndrome and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site irritation, application site reaction, application site urticaria, dizziness, nausea, sedation, . NEUPRO dosage: 2MG/24H,1 IN 1 D, TRANSDERMAL; 4MG/24H,1 IN 1 D, TRANSDERMAL. During the same period patient was treated with MIRAPEX, LEVOXYL, IRON OTC, CA OTC, VITAMIN C OTC, ASPIRIN, GLUCOSAMINE CHONDRAITIN OTC, LUNESTA. Patient recovered.