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Climara Side Effects Report #5646300-9
Health Professional from UNITED STATES reported CLIMARA problem on Jan 31, 2008. Female patient, 51 years of age, weighting 172.0 lb, was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site reaction, . CLIMARA dosage: unknown. During the same period patient was treated with ACIPHEX. Patient recovered.

Duragesic Side Effects Report #5647075-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 21, 2008. Female patient, weighting 140.0 lb, was diagnosed with pain, hypotonia and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site rash, back pain, dermatitis contact, eating disorder, feeling abnormal, lumbar puncture, neuralgia, . DURAGESIC dosage: unknown. During the same period patient was treated with VALIUM, KETOPROFEN. Patient recovered.

Arthritis Side Effects Report #5648727-8
Consumer or non-health professional from UNITED STATES reported ARTHRITIS HOT CHATHAM problem on Mar 03, 2008. Male patient, 31 years of age, weighting 235.0 lb, was diagnosed with back pain, intervertebral disc protrusion and was treated with ARTHRITIS HOT CHATHAM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, . ARTHRITIS HOT CHATHAM dosage: unknown. During the same period patient was treated with ARTHRITIS HOT CHATHAM. Patient was hospitalized and became disabled. 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.


Nicoderm Side Effects Report #5661682-X
Consumer or non-health professional from UNITED STATES reported NICODERM CQ problem on Mar 12, 2008. Female patient, 77 years of age, was treated with NICODERM CQ. After drug was administered, patient experienced the following problems/side effects: application site erythema, dizziness, loss of consciousness, . NICODERM CQ dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5663955-3
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Female patient, weighting 165.0 lb, was diagnosed with cancer pain, anxiety, sleep disorder, dyspepsia and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, constipation, hyperhidrosis, hypothyroidism, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with XANAX, AMBIEN, RANITIDINE. Patient recovered.

Ionsys Side Effects Report #5664102-4
Physician from GERMANY reported IONSYS problem on Mar 05, 2008. Female patient, 34 years of age, was diagnosed with arthrodesis, pain and was treated with IONSYS. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site reaction, application site vesicles, . IONSYS dosage: unknown. During the same period patient was treated with CONCOR, NOVALGIN, DEXAMETHASONE, RANTUDIL, MUSARIL, FOLSAN, MOVICOL. Patient recovered.

Neupro Side Effects Report #5664363-1
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2008. Male patient, 51 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 erythema, application site pruritus, no therapeutic response, pain, tremor, . NEUPRO dosage: 2MG/24H,1 IN 1 D,TRANSDERMAL;4MG/24H,1 IN 12 D,TRANSDERMAL;6MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with AZILECT. Patient recovered.

Neupro Side Effects Report #5664364-3
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Mar 04, 2008. Male patient, 61 years of age, weighting 215.0 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 erythema, application site pruritus, application site rash, eye pruritus, eyelid oedema, ocular hyperaemia, . NEUPRO dosage: 4MG/24H,1 IN 1; 6MG/24H,1 IN 1D,TRANSDERMAL. During the same period patient was treated with SINEMET. Patient recovered.


Neupro Side Effects Report #5664366-7
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Male patient, 78 years of age, weighting 135.0 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 erythema, application site irritation, application site pruritus, . NEUPRO dosage: 2MG/24H,1 IN 1 D,TRANSDERMAL; 4MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with CARBIDOPA AND LEVODOPA, MIDRODINE, AMITRIPTYLINE. Patient recovered.

Nicoderm Side Effects Report #5670386-9
Consumer or non-health professional from UNITED STATES reported NICODERM CQ problem 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.

Daytrana Side Effects Report #5670945-3
DAYTRANA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Female patient, child 11 years of age, weighting 69.89 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 erythema, application site rash, pneumonia, tic, . DAYTRANA dosage: 20 MG, 1X/DAY:QD, TRANSDERMAL. During the same period patient was treated with ADDERALL. Patient recovered.

Lamisil Side Effects Report #5671301-4
Consumer or non-health professional from BRAZIL reported LAMISIL problem on Feb 27, 2008. Female patient, 23 years of age, weighting 163.1 lb, was diagnosed with mycosis fungoides and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pain, blister, condition aggravated, dry skin, mycosis fungoides, pruritus, rash papular, . LAMISIL dosage: unknown. Patient recovered.

Catapres Side Effects Report #5671490-1
CATAPRES problem was reported by a Pharmacist from UNITED STATES on Feb 25, 2008. Male patient, weighting 185.2 lb, was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site rash, . CATAPRES dosage: unknown. During the same period patient was treated with SYNTHROID, NEXXIUM, AMLODIPINE, AVAPRO, FUROSEMIDE, LIPITOR, COREG. Patient recovered.


Catapres Side Effects Report #5677701-0
Pharmacist from UNITED STATES reported CATAPRES problem on Feb 27, 2008. Female patient, 66 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 erythema, application site rash, . CATAPRES dosage: unknown. During the same period patient was treated with ASPIRIN, PAPAVERINE SA, METOPROLOL SUCCINATE, FUROSEMIDE, SINGULAIR, ACTOS, AVAPRO, METFORMIN. Patient recovered.

Neupro Side Effects Report #5683237-3
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Male patient, 67 years of age, weighting 200.0 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, dyskinesia, feeling cold, micturition urgency, pollakiuria, sleep disorder, . 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 ASPIRIN, GLUCOSAMINE. Patient recovered.

Fentanyl Side Effects Report #5684416-1
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Mar 19, 2008. Female patient, weighting 132.0 lb, was diagnosed with arthralgia, depression, diarrhoea, tremor and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, application site rash, aspiration, cough, haematemesis, hyperhidrosis, malaise, nasopharyngitis, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FLUOXETINE, HALOPERIDOL, LOMOTIL, SINEMET. Patient recovered.

Emsam Side Effects Report #5685140-1
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 20, 2008. Female patient, weighting 214.0 lb, was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site erythema, dyskinesia, eyelid cyst, insomnia, migraine, pain, . EMSAM dosage: 12 MILLIGRAM , 1/1 DAY TD. During the same period patient was treated with METHAMPHETAMINE HYDROCHLORIDE, CHANTIX, NORCO, ZANAFLEX, ALBUTEROL, QVAR, CLARITIN, SYNTHROID. Patient died.

Neupro Side Effects Report #5691297-9
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Mar 13, 2008. Female patient, 68 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 pruritus, no therapeutic response, . NEUPRO dosage: 2MG/24H,1 IN 2 D,TRANSDERMAL; 4MG/24H,1 IN 1 D,TRANSDERMAL; 6MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with STOMATITS, ATENOLOL, AZILECT, PREMARIN. Patient recovered.


Duragesic Side Effects Report #5611826-0
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 25, 2008. Male patient, weighting 275.0 lb, was diagnosed with neuralgia, breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site erythema, depression, gastrooesophageal reflux disease, hypothyroidism, muscle spasms, neuralgia, . DURAGESIC dosage: unknown. During the same period patient was treated with ACTIQ. Patient recovered.

Altabax Side Effects Report #5619742-5
Consumer or non-health professional from UNITED STATES reported ALTABAX problem on Nov 30, 2007. Female patient, 70 years of age, was diagnosed with cyst and was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, application site pruritus, application site reaction, . ALTABAX dosage: unknown. Patient recovered.

Climara Side Effects Report #5621482-3
CLIMARA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 28, 2007. Female patient, 44 years of age, weighting 116.8 lb, was diagnosed with sleep disorder and was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site exfoliation, application site mass, . CLIMARA dosage: unknown. During the same period patient was treated with AMBIEN. Patient recovered.

Verdeso Side Effects Report #5623183-4
Physician from UNITED STATES reported VERDESO problem on Jan 28, 2008. Female patient was diagnosed with eczema and was treated with VERDESO. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, application site pain, . VERDESO dosage: unknown. Patient recovered.

Catapres Side Effects Report #5625101-1
CATAPRES problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2008. Male patient, child 7 years of age, was diagnosed with tic and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, . CATAPRES dosage: unknown. Patient recovered.

Niquitin Side Effects Report #5625961-4
Physician from UNITED KINGDOM reported NIQUITIN CQ CLEAR problem on Feb 11, 2008. Female patient, 43 years of age, was diagnosed with ex-smoker and was treated with NIQUITIN CQ CLEAR. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pain, eczema, hyperaesthesia, infection, nosocomial infection, staphylococcal infection, . NIQUITIN CQ CLEAR dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Nicorette Side Effects Report #5626582-X
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2008. Male patient, 53 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site erythema, blood glucose increased, blood pressure increased, pain in jaw, therapeutic response unexpected, toothache, treatment noncompliance, . NICORETTE dosage: unknown. During the same period patient was treated with NICOTINE, NICOTINE POLAXRILEX. Patient recovered.

Icyhot Side Effects Report #5628686-4
Consumer or non-health professional from UNITED STATES reported ICYHOT EXTRA STRENGHT CHATTEM problem on Feb 15, 2008. Male patient, 55 years of age, weighting 215.0 lb, was diagnosed with back pain and was treated with ICYHOT EXTRA STRENGHT CHATTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, application site pain, . ICYHOT EXTRA STRENGHT CHATTEM dosage: unknown. Patient recovered.

Finacea Side Effects Report #5629229-1
FINACEA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 13, 2007. Female patient, 38 years of age, weighting 108.0 lb, was diagnosed with acne and was treated with FINACEA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site inflammation, application site pruritus, cyst, scar, . FINACEA dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5630172-2
Physician from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 07, 2008. 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 erythema, 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.

Santyl Side Effects Report #5630327-7
SANTYL problem was reported by a Physician from UNITED STATES on Jan 29, 2008. Female patient, 71 years of age, was diagnosed with complex regional pain syndrome, ulcer and was treated with SANTYL. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site inflammation, application site pain, pseudomonas infection, wound infection staphylococcal, . SANTYL dosage: unknown. During the same period patient was treated with PREDNISONE, OMEPRAZOLE, PERCOCET, TRAZODONE, NOVOLOG, HYDROMORPHONE. Patient recovered.

Fentanyl Side Effects Report #5630714-7
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 08, 2008. Female patient, weighting 258.0 lb, was diagnosed with pain, inflammation, restless legs syndrome, type 2 diabetes mellitus and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, application site vesicles, convulsion, depression, insomnia, memory impairment, migraine, neuralgia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with DURAGESIC, LORTAB, CELEBREX, REQUIP, ACTOMET. Patient was hospitalized. Patient recovered.

Climara Side Effects Report #5634342-9
CLIMARA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 18, 2008. Female patient, 48 years of age, weighting 123.5 lb, was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site erythema, . CLIMARA dosage: unknown. Patient recovered.

Lamisil Side Effects Report #5635657-0
Consumer or non-health professional from BRAZIL reported LAMISIL problem on Feb 12, 2008. Female patient, 23 years of age, weighting 163.1 lb, was diagnosed with mycosis fungoides and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pain, blister, condition aggravated, dry skin, mycosis fungoides, pruritus, rash papular, . LAMISIL dosage: unknown. Patient recovered.

Icy Side Effects Report #5636618-8
ICY HOT STICK EXTRA ICY HOT problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2008. Female patient, 64 years of age, was diagnosed with pain and was treated with ICY HOT STICK EXTRA ICY HOT. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, . ICY HOT STICK EXTRA ICY HOT dosage: unknown. 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 #5637843-2
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2008. Male patient, 57 years of age, weighting 215.0 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 erythema, application site pruritus, application site rash, application site swelling, . NEUPRO dosage: 6MG / 24H, 1 IN 1 D, TRANSDERMAL; 2MG / 24H, 1 IN 1 D, TRANSDERMAL; 4MG / 24H, 1 IN 1 D, TRANSDERMAL. During the same period patient was treated with STALEVO, AMBIEN, AMANTADINE, FINASTERIDE, CELEBREX. Patient recovered.

Climara Side Effects Report #5637988-7
Consumer or non-health professional from UNITED STATES reported CLIMARA problem on Jan 16, 2008. Female patient, 57 years of age, weighting 200.6 lb, was diagnosed with anxiety, hypertension, hypothyroidism and was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, . CLIMARA dosage: unknown. During the same period patient was treated with EFFEXOR, TENORMIN, PRINZIDE, SYNTHROID. Patient recovered.

Duragesic Side Effects Report #5638013-4
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2008. Female patient, weighting 73.00 lb, was diagnosed with spinal column stenosis, breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site reaction, application site ulcer, dehydration, dyspnoea, myocardial infarction, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, LORTAB. Patient was hospitalized. Patient recovered.

Neupro Side Effects Report #5640766-6
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Feb 06, 2008. Male patient, 77 years of age, weighting 189.0 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 irritation, application site pruritus, . NEUPRO dosage: unknown. During the same period patient was treated with OXYCODONE AND ACETAMINOPHEN, LISINOPRIL. Patient recovered.

Nicorette Side Effects Report #5641350-0
NICORETTE problem was reported by a Consumer or non-health professional from UNITED STATES on June 26, 2007. Male patient, 35 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site excoriation, application site irritation, . NICORETTE dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Neupro Side Effects Report #5642021-7
Consumer or non-health professional from GERMANY reported NEUPRO problem on Jan 28, 2008. Male patient, 70 years of age, was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site exfoliation, application site pruritus, . NEUPRO dosage: 6 MG/24H (6 MG/24H 1 IN 1 DAY(S)) TRANSDERMAL. During the same period patient was treated with MADOPAR, LEVODOPA, ENTACAPONE, SOTALOL. Patient recovered.

Neupro Side Effects Report #5642024-2
NEUPRO problem was reported by a Consumer or non-health professional from GERMANY on Jan 02, 2008. Male patient, 64 years of age, was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, . NEUPRO dosage: 8 MG/24H (8 MG/24H 1 IN 1 DAY(S)) TRANSDERMAL. Patient recovered.

Fentanyl Side Effects Report #5645185-4
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 19, 2008. Female patient, weighting 170.0 lb, was diagnosed with pain, multiple sclerosis, bipolar disorder and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, device leakage, diabetes mellitus, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with LORTAB, BACLOFEN, LITHIUM CARBONATE, OXYCONTIN. Patient recovered.

Duragesic Side Effects Report #5645188-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Male patient, weighting 299.0 lb, was diagnosed with pain, breakthrough pain, fluid retention and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site scar, thrombosis, withdrawal syndrome, . DURAGESIC dosage: unknown. During the same period patient was treated with VICODIN, PERCOCET, HYDROCHLOROTHIAZIDE, DEMADEX. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5646431-3
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 28, 2008. Female patient, 60 years of age, weighting 162.0 lb, was diagnosed with neuropathy peripheral and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site pruritus, application site reaction, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient recovered.

Neupro Side Effects Report #5647961-0
NEUPRO problem was reported by a Pharmacist from UNITED STATES on Feb 14, 2008. Male patient, 51 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 erythema, application site pruritus, application site reaction, myalgia, pain, tremor, . NEUPRO dosage: 2MG/24G, 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 AZILECT. Patient recovered.

Fentanyl Side Effects Report #5578677-7
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Dec 21, 2007. Female patient, weighting 260.0 lb, was diagnosed with pain, breakthrough pain, diabetes mellitus, neuropathy peripheral and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, blood triglycerides increased, hyperglycaemia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with ULTRAM, HUMULIN R, HUMULIN R, LYRICA, NEURONTIN. Patient recovered.

Nicorette Side Effects Report #5581614-2
NICORETTE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Dec 28, 2007. Female patient, 26 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: application site erythema, dizziness, hyperhidrosis, malaise, nausea, visual disturbance, vomiting, . NICORETTE dosage: 10MG PER DAY. Patient recovered.

Fentanyl Side Effects Report #5583799-0
Physician from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Dec 27, 2007. Female patient, weighting 148.0 lb, was diagnosed with neuralgia and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site excoriation, burning sensation, fatigue, fibromyalgia, inadequate analgesia, rash, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with DURAGESIC, PEPCID, LEXAPRO. Patient recovered.

Daytrana Side Effects Report #5586209-2
DAYTRANA problem was reported by a Physician from UNITED STATES on Dec 26, 2007. Male patient, child 8 years of age, weighting 61.95 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 erythema, decreased appetite, disturbance in attention, hunger, increased appetite, mania, . DAYTRANA dosage: unknown. During the same period patient was treated with ZOLOFT. Patient recovered.

Scopoderm Side Effects Report #5589424-7
Consumer or non-health professional from UNITED KINGDOM reported SCOPODERM TTS problem on Dec 28, 2007. Male patient, 22 years of age, was diagnosed with salivary hypersecretion and was treated with SCOPODERM TTS. After drug was administered, patient experienced the following problems/side effects: application site erythema, application site irritation, convulsion, off label use, purulence, wound secretion, . SCOPODERM TTS dosage: unknown. During the same period patient was treated with GLUTAMINE, ASCORBIC ACID, PYRIDOXINE, ACIDIPHILUS, CLONAZEPAM, PHENYTOIN, ZONEGRAN, GLYCERIN SUPPOSITORIES. Patient recovered.