APPLICATION SITE DERMATITIS side effect
What is APPLICATION SITE DERMATITIS ?
Help Community - Describe Your Side Effect
Search FDA Side Effects
Ask Health Expert
APPLICATION SITE DERMATITIS and Recently Reported Side Effects
APPLICATION SITE DERMATITIS and 15 most Active Side Effect polls
APPLICATION SITE DERMATITIS and featured health surveys
Substances toxic to Health
Recent Hospital reviews
Comments about Side Effects
Hospital Quality reviews
Homecare Quality reviews
Drugs associated with APPLICATION SITE DERMATITIS
CATAPRES DAYTRANA EMSAM FENTANYL NEUPRO NICOTINE PROGRAFNeupro Side Effects Report #5642022-9
Consumer or non-health professional from GERMANY reported NEUPRO problem on Jan 21, 2008. Female patient, 65 years of age, was diagnosed with off label use, restless legs syndrome and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, . NEUPRO dosage: 4 MG/24H (4 MG/24H 1 IN 1 DAY(S)) TRANSDERMAL. Patient recovered.
Emsam Side Effects Report #5546079-5
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 25, 2007. Female patient, 62 years of age, weighting 191.8 lb, was diagnosed with major depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, insomnia, . EMSAM dosage: DOSE REDUCED TO 6MG/24HOURS. During the same period patient was treated with NEXIUM, AMBIEN, LEVOXYL. Patient recovered.
Fentanyl Side Effects Report #5528851-0
Physician from UNITED KINGDOM reported FENTANYL problem on Nov 21, 2007. Female patient, 87 years of age, was treated with FENTANYL. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, . FENTANYL dosage: unknown. During the same period patient was treated with ASPIRIN, CETIRIZINE, DIGOXIN, ISOSORBIDE MONONITRATE, LANSOPRAZOLE, LEVOTHYROXINE, PARACETAMOL, POTASSIUM PERMANGANATE. Patient was hospitalized. Patient recovered.
Nicotine Side Effects Report #5494465-4
NICOTINE problem was reported by a Physician from JAPAN on Oct 10, 2007. Male patient, 58 years of age, weighting 125.7 lb, was diagnosed with nicotine dependence and was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, gynaecomastia, nipple disorder, nipple swelling, . NICOTINE dosage: 21 MG; 14 MG; 7 MG QD, TRANSDERMAL. Patient recovered.
Nicotine Side Effects Report #5390773-6
Physician from FRANCE reported NICOTINE problem on July 06, 2007. Female patient, 42 years of age, weighting 116.8 lb, was diagnosed with tobacco withdrawal symptoms, surgery and was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, toxic skin eruption, . NICOTINE dosage: unknown. During the same period patient was treated with NICORETTE, BETADINE. Patient recovered.
Nicotine Side Effects Report #5390773-6
NICOTINE problem was reported by a Physician from FRANCE on July 06, 2007. Female patient, 42 years of age, weighting 116.8 lb, was diagnosed with tobacco withdrawal symptoms, surgery and was treated with NICOTINE. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, toxic skin eruption, . NICOTINE dosage: unknown. During the same period patient was treated with NICORETTE, BETADINE. Patient recovered.
Neupro Side Effects Report #5676748-8
Health Professional from UNITED STATES reported NEUPRO problem on Jan 08, 2008. Male patient was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, application site reaction, . NEUPRO dosage: 6MG/24H, 1 IN 1 D,TRANSDERMAL. Patient recovered.
Neupro Side Effects Report #5676780-4
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 04, 2008. Male patient, 57 years of age, weighting 200.0 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 dermatitis, application site erythema, application site rash, application site reaction, blood pressure increased, dizziness, dry skin, . NEUPRO dosage: 2MG/24H, 1 IN 1; 4 MG/24H, 1 IN 1 D; 6MG/24H, 1 IN 1D; 4 MG/24H, 1 IN 1 D, TRANDERMAL. During the same period patient was treated with COENZYME Q. Patient recovered.
Daytrana Side Effects Report #5366058-0
Physician from UNITED STATES reported DAYTRANA problem on Dec 21, 2006. Male patient was diagnosed with psychomotor hyperactivity and was treated with DAYTRANA. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, application site vesicles, . DAYTRANA dosage: 20 MG EVERY MORNING, TRANSDERMAL. Patient recovered.
Prograf Side Effects Report #5339458-2
PROGRAF problem was reported by a Physician from JAPAN on May 14, 2007. Male patient, child 7 years of age, weighting 35.27 lb, was diagnosed with dermatitis atopic and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: application site dermatitis, condition aggravated, dermatitis atopic, disease recurrence, eczema impetiginous, . PROGRAF dosage: unknown. During the same period patient was treated with AZUNOL #, AZUNOL #. Patient was hospitalized. Patient recovered.
Catapres Side Effects Report #5543802-0
Physician from UNITED STATES reported CATAPRES problem on Nov 16, 2007. Female patient, 75 years of age, weighting 145.5 lb, was diagnosed with hypertension and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: anxiety, application site dermatitis, application site irritation, application site pruritus, blood pressure inadequately controlled, . CATAPRES dosage: unknown. During the same period patient was treated with DYNACIRC CR, GINKO BILOBA, LASIX, LORAZEPAM, LOZOL, CARDURA, POTASSIUM CHLORIDE. Patient recovered.
Catapres Side Effects Report #5567238-1
CATAPRES problem was reported by a Physician from UNITED STATES on Dec 18, 2007. Female patient, 75 years of age, weighting 145.5 lb, was diagnosed with hypertension and was treated with CATAPRES. After drug was administered, patient experienced the following problems/side effects: anxiety, application site dermatitis, application site irritation, application site pruritus, blood pressure inadequately controlled, . CATAPRES dosage: unknown. During the same period patient was treated with DYNACIRC CR, GINKO BILOBA, LASIX, LORAZEPAM, LOZOL, CARDURA, POTASSIUM CHLORIDE. Patient recovered.