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APPLICATION SITE PRURITUS side effect

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Duragesic Side Effects Report #5657081-7
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 28, 2008. Female patient, weighting 151.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, bronchitis, cerebrovascular accident, memory impairment, transient ischaemic attack, . DURAGESIC dosage: unknown. Patient was hospitalized. Patient recovered.

Nicorette Side Effects Report #5663818-3
NICORETTE problem was reported by a Health Professional from DENMARK on Feb 27, 2008. Female patient was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site pruritus, cold sweat, malaise, . NICORETTE 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.

Duragesic Side Effects Report #5675586-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Male patient, weighting 270.0 lb, was diagnosed with arthritis, pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, diabetes mellitus, myocardial infarction, . DURAGESIC dosage: unknown. During the same period patient was treated with VICODIN ES. Patient was hospitalized. Patient recovered.


Neupro Side Effects Report #5678720-0
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Mar 05, 2008. Female patient, 77 years of age, weighting 138.0 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 rash, dermatitis contact, . NEUPRO dosage: 4 MG/24H, 1 IN 1 D, TRANSDERMAL; 2MG/24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with HYDROCHLOROTHIAZIDE, SIMVASTATIN. Patient recovered.

Neupro Side Effects Report #5679680-9
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Male patient was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site reaction, rash maculo-papular, . NEUPRO dosage: 6MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Neupro Side Effects Report #5679684-6
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Mar 11, 2008. Male patient was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, application site reaction, . NEUPRO dosage: 6MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Neupro Side Effects Report #5679685-8
NEUPRO problem was reported by a Health Professional from UNITED STATES on Mar 11, 2008. Male patient was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, . NEUPRO dosage: 6MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Neupro Side Effects Report #5679689-5
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Mar 11, 2008. Male patient was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, . NEUPRO dosage: 6 MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.


Neupro Side Effects Report #5679690-1
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Male patient was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, . NEUPRO dosage: 6MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Climara Side Effects Report #5614915-X
Consumer or non-health professional from UNITED STATES reported CLIMARA problem on Dec 14, 2007. Female patient, 43 years of age, was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, breast enlargement, 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.

Fentanyl Side Effects Report #5618638-2
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Physician from UNITED STATES on Jan 29, 2008. Female patient, weighting 161.0 lb, was diagnosed with pain, kyphosis, dyspepsia, blood pressure, diabetes mellitus, migraine and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, blood cholesterol increased, blood pressure increased, dermatitis contact, diabetes mellitus, insomnia, migraine, rash, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, DURAGESIC, PROTONIX, CARDIZEM CD, METFORMIN, KEPPRA. Patient recovered.


Neupro Side Effects Report #5637842-0
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Feb 07, 2008. Male patient, 77 years of age, weighting 145.5 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 rash, asthenia, confusional state, decreased activity, hallucination, . NEUPRO dosage: unknown. During the same period patient was treated with ACIPHEX, PLAVIX, FLOMAX, VERAPAMIL. Patient recovered.

Duragesic Side Effects Report #5642452-5
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Female patient, weighting 236.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, arthralgia, bedridden, condition aggravated, female sterilisation, hyperhidrosis, hypersomnia, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM. Patient recovered.

Elidel Side Effects Report #5662017-9
Consumer or non-health professional from UNITED STATES reported ELIDEL problem 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.

Fentanyl Side Effects Report #5584358-6
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Physician from UNITED STATES on Jan 03, 2008. Female patient, weighting 161.0 lb, was diagnosed with pain, kyphosis, dyspepsia, blood pressure, diabetes mellitus, migraine and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, blister, blood cholesterol increased, blood pressure increased, dermatitis contact, diabetes mellitus, insomnia, migraine, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, DURAGESIC, PROTONIX, CARDIZEM CD, METFORMIN, KEPPRA. Patient recovered.

Fentanyl Side Effects Report #5584359-8
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Dec 28, 2007. Male patient, weighting 195.0 lb, was diagnosed with back pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, blood cholesterol increased, diabetes mellitus, hypertension, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, DURAGESIC. Patient recovered.


Duragesic Side Effects Report #5587942-9
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 02, 2008. Female patient, weighting 236.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, arthralgia, bedridden, condition aggravated, female sterilisation, hyperhidrosis, hypersomnia, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM. Patient recovered.

Duragesic Side Effects Report #5594425-9
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Jan 08, 2008. Male patient, weighting 290.0 lb, was diagnosed with pain, hypogonadism, gastrooesophageal reflux disease, hypertension and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, back pain, blood triglycerides increased, diabetes mellitus, hypertension, neuropathy peripheral, . DURAGESIC dosage: unknown. During the same period patient was treated with TESTOSTERONE, NEXIUM, PROPRANOLOL, ANDROGEL. Patient recovered.

Duragesic Side Effects Report #5600268-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 15, 2008. Female patient, weighting 236.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, arthralgia, bedridden, condition aggravated, female sterilisation, hyperhidrosis, hypersomnia, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM. Patient recovered.

Nicoderm Side Effects Report #5546359-3
Consumer or non-health professional from UNITED STATES reported NICODERM CQ problem on Dec 06, 2007. Female patient, 28 years of age, weighting 130.0 lb, was treated with NICODERM CQ. After drug was administered, patient experienced the following problems/side effects: application site pruritus, choking, dyspnoea, fear, laryngospasm, pain in extremity, . NICODERM CQ dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5564801-9
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2007. Female patient, weighting 210.0 lb, was diagnosed with osteoporosis, fibromyalgia, pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site reaction, application site vesicles, diabetes mellitus, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, METHADONE, LASIX. Patient recovered.

Rogaine Side Effects Report #5581122-9
Consumer or non-health professional from UNITED STATES reported ROGAINE EXTRA STRENGTH problem on Dec 19, 2007. Female patient, 74 years of age, weighting 138.0 lb, was diagnosed with alopecia and was treated with ROGAINE EXTRA STRENGTH. After drug was administered, patient experienced the following problems/side effects: application site pruritus, blood pressure increased, . ROGAINE EXTRA STRENGTH dosage: 1 ML TWICE DAILY (2 IN 1 D), TOPICAL. During the same period patient was treated with SYNTHROID, DETROL, FOSAMAX, CALCIUM, VITAMIN C. Patient recovered.

Neupro Side Effects Report #5588834-1
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 11, 2007. Female patient, 68 years of age, weighting 207.2 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 rash, . NEUPRO dosage: 2MG/24H,1 IN 1 D,TRANSDERMAL ; 6MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with AZILECT, STALEVO, HUMALOG, LANTUS, HYDROCORTISONE. Patient recovered.

Hance Side Effects Report #5592414-1
Health Professional from UNITED STATES reported HANCE problem on Sept 24, 2007. Female patient was diagnosed with nuclear magnetic resonance imaging and was treated with HANCE. After drug was administered, patient experienced the following problems/side effects: application site pruritus, chest discomfort, hypertension, nausea, tremor, . HANCE dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5503714-5
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 24, 2007. Male patient, weighting 230.0 lb, was diagnosed with back pain, blood pressure and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, emphysema, weight decreased, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with LISINOPRIL, FOSAMAX, ASPIRIN, COREG, LIPITOR. Patient recovered.

Fentanyl Side Effects Report #5511031-2
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Oct 30, 2007. Female patient, weighting 161.0 lb, was diagnosed with kyphosis, dyspepsia, blood pressure, diabetes mellitus, migraine and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, blood cholesterol increased, blood pressure increased, dermatitis contact, diabetes mellitus, insomnia, migraine, vaginal haemorrhage, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with DURAGESIC, PROTONIX, CARDIZEM CD, METFORMIN, KEPPRA. Patient recovered.

Commit Side Effects Report #5517075-9
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 06, 2007. Female patient, 40 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site pruritus, arthralgia, asthenia, discomfort, feeling abnormal, headache, hypersomnia, myalgia, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Fentanyl Side Effects Report #5519084-2
Health Professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Nov 05, 2007. Female patient, weighting 185.0 lb, was diagnosed with pain, asthma and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, cerebrovascular accident, complex regional pain syndrome, depression, heart rate irregular, hip surgery, hypertension, insomnia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, ALBUTEROL, SINGULAIR. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5521048-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 08, 2007. Female patient, weighting 162.0 lb, was diagnosed with back pain, anxiety, chest pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, breakthrough pain, cardiac failure, gastric disorder, nervousness, . DURAGESIC dosage: unknown. During the same period patient was treated with LORAZEPAM, NITROGLYCERIN. Patient was hospitalized. Patient recovered.

Nicorette Side Effects Report #5524815-1
Consumer or non-health professional from UNITED KINGDOM reported NICORETTE problem on Nov 08, 2007. Female patient was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site pruritus, dyspnoea, pharyngeal hypoaesthesia, . NICORETTE dosage: 15MG, TRANSDERMAL. Patient recovered.

Bactroban Side Effects Report #5530619-6
BACTROBAN problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Female patient, 82 years of age, was diagnosed with skin infection and was treated with BACTROBAN. After drug was administered, patient experienced the following problems/side effects: application site pruritus, visual acuity reduced, . BACTROBAN dosage: unknown. Patient recovered.

Catapres Side Effects Report #5485910-9
Consumer or non-health professional from UNITED STATES reported CATAPRES problem on Sept 27, 2007. Female patient, 93 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 pruritus, blood pressure increased, . CATAPRES dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, HYDROCORTISONE, ANTIVERT. Patient recovered.

Efudex Side Effects Report #5522918-9
EFUDEX problem was reported by a Pharmacist from UNITED STATES on July 17, 2007. Female patient was treated with EFUDEX. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, blood creatine phosphokinase increased, . EFUDEX dosage: unknown. Patient recovered.

Catapres Side Effects Report #5445472-9
Consumer or non-health professional from UNITED STATES reported CATAPRES problem on Aug 21, 2007. Female patient, 93 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 pruritus, blood pressure increased, . CATAPRES dosage: unknown. Patient recovered.

Ortho Side Effects Report #5447220-5
ORTHO EVRA problem was reported by a Consumer or non-health professional from BRAZIL on Aug 29, 2007. Female patient, 25 years of age, weighting 121.3 lb, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: application site pruritus, hepatitis c, rash macular, . ORTHO EVRA dosage: unknown. During the same period patient was treated with HIXIZINE. Patient recovered.

Duragesic Side Effects Report #5452324-7
Physician from UNITED STATES reported DURAGESIC problem on Sept 04, 2007. Male patient, weighting 190.0 lb, was diagnosed with surgery, pain, blood pressure and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, arachnoiditis, inadequate analgesia, muscle spasms, . DURAGESIC dosage: unknown. During the same period patient was treated with LORTAB, TENORMIN. Patient recovered.

Catapres Side Effects Report #5453029-9
CATAPRES problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 05, 2007. Male patient, child 10 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site pruritus, . CATAPRES dosage: unknown. During the same period patient was treated with RISPERIDONE, SYNTHROID, FOCALIN. Patient recovered.

Catapres Side Effects Report #5457608-4
Consumer or non-health professional from UNITED STATES reported CATAPRES problem on Sept 06, 2007. Male patient, 83 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 pruritus, application site rash, . CATAPRES dosage: unknown. During the same period patient was treated with ATENOLOL, LISINOPRIL, FOLIC ACID, NORVASC, MICARDIS. Patient recovered.

Abreva Side Effects Report #5461603-9
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2006. Female patient, 43 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pruritus, hypersensitivity, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461693-3
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Dec 04, 2006. Female patient, 85 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pruritus, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462363-8
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, 41 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pruritus, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Lioresal Side Effects Report #5463533-5
Consumer or non-health professional from UNITED STATES reported LIORESAL problem on Sept 05, 2007. Female patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: application site pruritus, dysuria, feeling of body temperature change, formication, hyperhidrosis, micturition urgency, muscle rigidity, . LIORESAL dosage: unknown. During the same period patient was treated with ORAL BENADRYL. Patient recovered.

Duragesic Side Effects Report #5408147-8
DURAGESIC problem was reported by a Physician from UNITED STATES on July 30, 2007. Male patient, weighting 190.0 lb, was diagnosed with surgery, pain, blood pressure and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, arachnoiditis, inadequate analgesia, muscle spasms, . DURAGESIC dosage: unknown. During the same period patient was treated with LORTAB, TENORMIN. Patient recovered.

Fentanyl Side Effects Report #5425068-5
Health Professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Aug 15, 2007. Female patient, weighting 185.0 lb, was diagnosed with pain, asthma and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, cerebrovascular accident, complex regional pain syndrome, depression, heart rate irregular, hip surgery, hypertension, insomnia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, ALBUTEROL, SINGULAIR. Patient was hospitalized. Patient recovered.

Zovirax Side Effects Report #5428819-9
ZOVIRAX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2007. Female patient, 82 years of age, was diagnosed with pain and was treated with ZOVIRAX. After drug was administered, patient experienced the following problems/side effects: application site pruritus, . ZOVIRAX dosage: unknown. During the same period patient was treated with VICODIN, COZAAR, DIGOXIN, HYDROCHLOROTHIAZIDE, POTASSIUM CHLORIDE, PRILOSEC, WARFARIN. Patient recovered.

Catapres Side Effects Report #5429943-7
Physician from UNITED STATES reported CATAPRES problem on July 09, 2007. Female patient, weighting 299.8 lb, was diagnosed with hypertension and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site pruritus, application site rash, application site vesicles, blood pressure systolic increased, feeling jittery, irritability, memory impairment, nervousness, somnolence, . CATAPRES dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, NORVASC, COREG, LASIX, HYZAAR, METHOTREXATE, PEPCID. Patient recovered.

Transderm Side Effects Report #5383793-9
TRANSDERM SCOP problem was reported by a Pharmacist from UNITED STATES on June 27, 2007. Male patient, child 5 years of age, weighting 44.97 lb, was diagnosed with drooling and was treated with TRANSDERM SCOP. After drug was administered, patient experienced the following problems/side effects: application site pruritus, eye swelling, grand mal convulsion, oedema peripheral, pyrexia, rash, urticaria, . TRANSDERM SCOP dosage: 1.5 MG, Q72H, TRANSDERMAL. During the same period patient was treated with TRANSDERM SCOP, VITAMINS, MIRALAX, FOCALIN, PREVACID, ADVAIR DISKUS, ELIDEL, NASONEX. Patient recovered.

Duragesic Side Effects Report #5385191-0
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on July 02, 2007. Female patient, weighting 113.0 lb, was diagnosed with pain, contraception, pancreatic enzymes, nutritional support, nausea, asthma and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site pruritus, pain, pancreatitis chronic, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, CREON, SUPPLEMENT, ZOFRAN, PROVENTIL. Patient was hospitalized. Patient recovered.