APPLICATION SITE REACTION side effect
What is APPLICATION SITE REACTION ?Drugs associated with APPLICATION SITE REACTION
ABREVA AGGRENOX ALTABAX BENGAY CATAPRES CHLORAPREP CLIMARA CLOBETASOL CLOTRIMAZOLE COMMIT DURAGESIC EMSAM ENBREL ESTRADERM FENTANYL GOLD IMITREX IONSYS KENTERA LUTENYL METVIX MIRENA NEUPRO NICOTINE NITRO PROTOPIC STRIANT TARGET VISINE VOLTAREN XALATAN ZOVIRAXAPPLICATION SITE REACTION : Clotrimazole Side Effects Report #5650883-2
Health Professional from UNITED KINGDOM reported CLOTRIMAZOLE problem on Feb 25, 2008. Female patient, 20 years of age, was diagnosed with tinea infection, contraception and was treated with CLOTRIMAZOLE. After drug was administered, patient experienced the following problems/side effects: application site reaction, muscle spasms, . CLOTRIMAZOLE dosage: unknown. During the same period patient was treated with CERAZETTE. Patient recovered.
APPLICATION SITE REACTION : Striant Side Effects Report #5657209-9
STRIANT problem was reported by a Physician from UNITED STATES on Mar 07, 2008. Male patient, 25 years of age, weighting 153.7 lb, was diagnosed with androgen deficiency and was treated with STRIANT. After drug was administered, patient experienced the following problems/side effects: application site reaction, gingival atrophy, . STRIANT dosage: 30 MG EVERY 12 HOURS BUCCAL. Patient recovered.
APPLICATION SITE REACTION : Fentanyl Side Effects Report #5662832-1
Consumer or non-health professional from UNITED STATES reported FENTANYL problem on Feb 22, 2008. Female patient, 54 years of age, weighting 182.0 lb, was diagnosed with pain and was treated with FENTANYL. After drug was administered, patient experienced the following problems/side effects: application site reaction, blood pressure decreased, choking, convulsion, dizziness, dysphagia, dyspnoea, feeling abnormal, loss of consciousness, . FENTANYL dosage: unknown. During the same period patient was treated with XANAX, ELAVIL, CYCLOBENZAPRINE, GABAPENTIN, PREMARIN, IRON, PREVACID. Patient recovered.
APPLICATION SITE REACTION : Mirena Side Effects Report #5681960-8
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 30, 2007. Female patient, 49 years of age, weighting 160.9 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: application site reaction, burning sensation, complication of device insertion, . MIRENA dosage: unknown. During the same period patient was treated with WELLBUTRIN, TOPEX, ALLEGRA. Patient recovered.
APPLICATION SITE REACTION : Protopic Side Effects Report #5616165-X
Physician from JAPAN reported PROTOPIC problem on Jan 16, 2008. Male patient, child 4 years of age, weighting 478.4 lb, was diagnosed with dermatitis atopic and was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: application site reaction, impetigo, kaposi's varicelliform eruption, . PROTOPIC dosage: unknown. During the same period patient was treated with KINDAVATE. Patient recovered.
APPLICATION SITE REACTION : Aggrenox Side Effects Report #5625520-3
AGGRENOX problem was reported by a Physician from UNITED STATES on Feb 11, 2008. Female patient, 80 years of age, was treated with AGGRENOX. After drug was administered, patient experienced the following problems/side effects: application site reaction, breast haematoma, . AGGRENOX dosage: unknown. During the same period patient was treated with NITROGLYCERIN. Patient recovered.
APPLICATION SITE REACTION : Chloraprep Side Effects Report #5634149-2
Consumer or non-health professional from UNITED STATES reported CHLORAPREP problem on Feb 21, 2008. Female patient, 45 years of age, was treated with CHLORAPREP. After drug was administered, patient experienced the following problems/side effects: application site reaction, blister, erythema, . CHLORAPREP dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Protopic Side Effects Report #5636222-1
PROTOPIC problem was reported by a Physician from FRANCE on Jan 30, 2008. Female patient, 13 years of age, was diagnosed with dermatitis atopic and was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: application site reaction, lentigo, malignant melanoma, . PROTOPIC dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Imitrex Side Effects Report #5638641-6
Consumer or non-health professional from UNITED STATES reported IMITREX problem on July 25, 2007. Female patient, 52 years of age, was diagnosed with migraine and was treated with IMITREX. After drug was administered, patient experienced the following problems/side effects: application site reaction, nausea, pain, . IMITREX dosage: 6MG AS REQUIRED. During the same period patient was treated with LOPRESSOR. Patient recovered.
APPLICATION SITE REACTION : Duragesic Side Effects Report #5578813-2
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 21, 2007. Female patient, weighting 125.0 lb, was diagnosed with pain, unevaluable event, mitral valve prolapse, fibromyalgia and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site reaction, unevaluable event, . DURAGESIC dosage: unknown. During the same period patient was treated with PREDNISONE, PREMARIN, CARDIZEM, CELEBREX, VICODIN, ULTRAM, PROCARDIA. Patient recovered.
APPLICATION SITE REACTION : Protopic Side Effects Report #5584687-6
Physician from FRANCE reported PROTOPIC problem on Dec 18, 2007. Female patient, 13 years of age, was diagnosed with dermatitis atopic and was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: application site reaction, lentigo, malignant melanoma, . PROTOPIC dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Duragesic Side Effects Report #5593129-6
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 07, 2008. Male patient was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site reaction, device failure, feeling abnormal, myocardial infarction, . DURAGESIC dosage: unknown. During the same period patient was treated with VICODIN, VALIUM. Patient was hospitalized. Patient recovered.
APPLICATION SITE REACTION : Voltaren Side Effects Report #5597154-0
Consumer or non-health professional from FRANCE reported VOLTAREN problem on Jan 10, 2008. Female patient, 21 years of age, was diagnosed with back pain and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: application site reaction, blood urine present, c-reactive protein increased, eosinophil count abnormal, erythema, leukocyturia, nitrite urine absent, oedema peripheral, pruritus, . VOLTAREN dosage: unknown. During the same period patient was treated with NIFLURIL, TETRAZEPAM. Patient was hospitalized. Patient recovered.
APPLICATION SITE REACTION : Neupro Side Effects Report #5610421-7
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Male patient, 69 years of age, weighting 185.0 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, erythema, pruritus, urticaria, . NEUPRO dosage: 6MG/24H,1 IN 1 D,TRANSDERMAL;4MG/24H,1 IN 1D,TRANSDERMAL;2MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with ARTANE, AZILECT, LIPITOR, ACTONEL. Patient recovered.
APPLICATION SITE REACTION : Kentera Side Effects Report #5614864-7
Health Professional from UNITED KINGDOM reported KENTERA problem on Jan 24, 2008. Female patient, 37 years of age, weighting 299.8 lb, was diagnosed with urinary incontinence and was treated with KENTERA. After drug was administered, patient experienced the following problems/side effects: application site reaction, myalgia, . KENTERA dosage: unknown. During the same period patient was treated with CETIRIZINE, DIAZEPAM, MEBEVERINE, OMEPRAZOLE, PAROXETINE. Patient recovered.
APPLICATION SITE REACTION : Zovirax Side Effects Report #5535708-8
ZOVIRAX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 04, 2007. Female patient, 48 years of age, weighting 127.0 lb, was diagnosed with oral herpes and was treated with ZOVIRAX. After drug was administered, patient experienced the following problems/side effects: application site reaction, condition aggravated, infection, skin disorder, . ZOVIRAX dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Duragesic Side Effects Report #5537002-8
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Nov 27, 2007. Female patient, weighting 238.0 lb, was diagnosed with back pain, depression, neuropathy, urinary tract disorder and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site reaction, blood pressure increased, catheterisation cardiac, . DURAGESIC dosage: unknown. During the same period patient was treated with EFFEXOR, LEXOXYL, BACLOFEN, POTASSIUM CHLORIDE, FLOMAX. Patient was hospitalized. Patient recovered.
APPLICATION SITE REACTION : Fentanyl Side Effects Report #5537710-9
FENTANYL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Male patient, weighting 162.0 lb, was diagnosed with pain in extremity, nerve injury and was treated with FENTANYL. After drug was administered, patient experienced the following problems/side effects: application site reaction, dizziness, dyspnoea, gait disturbance, headache, heart rate irregular, hypoaesthesia, lip swelling, nausea, . FENTANYL dosage: unknown. During the same period patient was treated with PERCOCET, VALIUM, LYRICA. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546027-8
Consumer or non-health professional from UNITED STATES reported EMSAM problem on Sept 17, 2007. Female patient, 58 years of age, weighting 119.0 lb, was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, weight increased, . EMSAM dosage: CURRENT DOSE OF SELIGILINE TRANSDERMAL PATCH IS 9 MG.. During the same period patient was treated with LISINOPRIL, CLONAZEPAM, SEROQUEL, PREVACID. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546029-1
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2007. Female patient, 21 years of age, was diagnosed with bipolar disorder and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: unknown. During the same period patient was treated with DEPAKOTE, LITHIUM CARBONATE, ROZEREM. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546038-2
Consumer or non-health professional from UNITED STATES reported EMSAM problem on Aug 27, 2007. Female patient was diagnosed with depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: unknown. During the same period patient was treated with VIVELLE. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546043-6
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2007. Female patient, 57 years of age, weighting 134.5 lb, was diagnosed with depression, anxiety and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: unknown. During the same period patient was treated with SYNTHROID, VIVELLE. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546049-7
Consumer or non-health professional from UNITED STATES reported EMSAM problem on Sept 05, 2007. Female patient, 66 years of age, weighting 143.3 lb, was diagnosed with depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: PATIENT ALSO USED 6MG/24HR AND 9MG/24HR PATCHES .. During the same period patient was treated with ALPRAZOLAM, DIOVAN HCT, LEVOXYL. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546061-8
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2007. Female patient, 30 years of age, weighting 229.3 lb, was diagnosed with bipolar disorder, depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, menorrhagia, . EMSAM dosage: unknown. During the same period patient was treated with LITHIUM CARBONATE, INVEGA. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546069-2
Health Professional from UNITED STATES reported EMSAM problem on Sept 20, 2007. Female patient, 58 years of age, was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: STARTED AS 12MG/24HOUR ON 11/2006 WHICH WAS LOWERED TO 6MG/24HOUR ON 07/2007.. During the same period patient was treated with KLONOPIN. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546075-8
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Female patient, 66 years of age, weighting 172.0 lb, was diagnosed with nervousness and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, hypersensitivity, . EMSAM dosage: EMSAM 20 MG/24 HR TRANSDERMAL PATCH.. During the same period patient was treated with HYZAAR, DICYCLOMINE, ALPRAZOLAM, VITAMIN B, XALATAN, CLIMARA, XANAX. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546082-5
Consumer or non-health professional from UNITED STATES reported EMSAM problem on Sept 27, 2007. Female patient, 57 years of age, weighting 138.9 lb, was diagnosed with major depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: DOSE INCREASED ON 24AUG07 TO 9MG/24HRS AND ON 21SEP07,6MG/24HR,2PATCHES. During the same period patient was treated with PROVIGIL, TOPROL, NORVASC, DEPIN, VITAMIN B CAP, ASCORBIC ACID, EPA DHA. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546083-7
EMSAM problem was reported by a Physician from UNITED STATES on Sept 27, 2007. Female patient, 54 years of age, weighting 220.5 lb, was diagnosed with major depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: INTIAL DOSE OF 6MG ON 17 JUL 2007. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546084-9
Consumer or non-health professional from UNITED STATES reported EMSAM problem on Sept 28, 2007. Female patient, 61 years of age, weighting 136.7 lb, was diagnosed with depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: unknown. During the same period patient was treated with TYLENOL, XANAX. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546095-3
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 08, 2007. Female patient was diagnosed with depression and was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: DOSE WAS INCREASED TO 9MG. During the same period patient was treated with ALPRAZOLAM, RISPERDAL. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546101-6
Physician from UNITED STATES reported EMSAM problem on Oct 10, 2007. Female patient was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546108-9
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 17, 2007. Female patient was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, oedema peripheral, . EMSAM dosage: unknown. During the same period patient was treated with XANAX, LEVOXYL, COZAAR. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546112-0
Physician from UNITED STATES reported EMSAM problem on Oct 24, 2007. Female patient was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Emsam Side Effects Report #5546132-6
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2007. Male patient was treated with EMSAM. After drug was administered, patient experienced the following problems/side effects: application site reaction, . EMSAM dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Protopic Side Effects Report #5565840-4
Physician from FRANCE reported PROTOPIC problem on Nov 29, 2007. Female patient, 13 years of age, was diagnosed with dermatitis atopic and was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: application site reaction, lentigo, lymphadenopathy, malignant melanoma, . PROTOPIC dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Lutenyl Side Effects Report #5568364-3
LUTENYL problem was reported by a Consumer or non-health professional from FRANCE on Dec 13, 2007. Female patient was treated with LUTENYL. After drug was administered, patient experienced the following problems/side effects: application site reaction, asthma, chest pain, headache, herpes zoster, hormone level abnormal, hot flush, hypertrichosis, malaise, . LUTENYL dosage: unknown. During the same period patient was treated with ESTRADERM. Patient recovered.
APPLICATION SITE REACTION : Nitro Side Effects Report #5582842-2
Physician from ITALY reported NITRO problem on Dec 19, 2007. Male patient, 62 years of age, was diagnosed with myocardial ischaemia and was treated with NITRO. After drug was administered, patient experienced the following problems/side effects: application site reaction, cellulitis, erythema, mediastinitis, muscle swelling, neutrophilia, pain, purulent discharge, pyrexia, . NITRO dosage: unknown. Patient was hospitalized. Patient recovered.
APPLICATION SITE REACTION : Neupro Side Effects Report #5587795-9
NEUPRO problem was reported by a Physician from UNITED STATES on Oct 26, 2007. Male patient, 74 years of age, weighting 173.0 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 reaction, . NEUPRO dosage: 4MG/24H,1 IN 1 D,TRANSDERMAL ; 2MG/24H,1 IN 1 D,TRANSDERMAL. Patient recovered.
APPLICATION SITE REACTION : Neupro Side Effects Report #5587865-5
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Sept 24, 2007. Male patient 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, pollakiuria, tremor, . NEUPRO dosage: 4MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with NEXIUM. Patient recovered.
APPLICATION SITE REACTION : Neupro Side Effects Report #5588944-9
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 17, 2007. Female patient, 62 years of age, weighting 165.3 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, tinnitus, . NEUPRO dosage: 2MG/24H,1 IN 1 D,TRANSDERMAL. During the same period patient was treated with SINEMET CR. Patient recovered.
APPLICATION SITE REACTION : Neupro Side Effects Report #5588946-2
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Oct 23, 2007. Male patient, 72 years of age, weighting 200.6 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, . 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 AZILECT, LISINOPRIL, GLYBURIDE, LASIX, TOPROL, SINEMET. Patient recovered.
APPLICATION SITE REACTION : Neupro Side Effects Report #5588954-1
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 30, 2007. Female patient, 52 years of age, was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: application site reaction, application site scar, hallucination, . NEUPRO dosage: unknown. During the same period patient was treated with SINEMET, TASMAR. Patient recovered.
APPLICATION SITE REACTION : Gold Side Effects Report #5507239-2
Consumer or non-health professional from UNITED STATES reported GOLD BOND HEALING MEDICATED BODY problem on Nov 05, 2007. Male patient, weighting 170.0 lb, was treated with GOLD BOND HEALING MEDICATED BODY. After drug was administered, patient experienced the following problems/side effects: application site reaction, caustic injury, melanocytic naevus, naevus haemorrhage, orchitis noninfective, swelling, testicular pain, testicular swelling, . GOLD BOND HEALING MEDICATED BODY dosage: unknown. During the same period patient was treated with GOLD BOND HEALING MEDICATED BODY, GOLD BOND HEALING MEDICATED BODY. Patient recovered.
APPLICATION SITE REACTION : Estraderm Side Effects Report #5511150-0
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 02, 2007. Female patient, 26 years of age, weighting 116.8 lb, was diagnosed with ovarian failure, osteoporosis, eczema, depression and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: application site reaction, nausea, night sweats, pain, . ESTRADERM dosage: unknown. During the same period patient was treated with BONIVA, ACRIVASTINE, CITALOPRAM. Patient recovered.
APPLICATION SITE REACTION : Altabax Side Effects Report #5511368-7
Consumer or non-health professional from UNITED STATES reported ALTABAX problem on Sept 26, 2007. Female patient was diagnosed with impetigo and was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site reaction, . ALTABAX dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Commit Side Effects Report #5516177-0
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 04, 2007. Female patient, 49 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site reaction, diarrhoea, hypersensitivity, irritable bowel syndrome, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.
APPLICATION SITE REACTION : Commit Side Effects Report #5516470-1
Consumer or non-health professional from UNITED STATES reported COMMIT problem on Mar 01, 2007. Male patient, 61 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site reaction, diarrhoea, malaise, vomiting, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.
APPLICATION SITE REACTION : Visine Side Effects Report #5523251-1
VISINE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2007. Female patient, 23 years of age, weighting 200.0 lb, was diagnosed with eye pruritus and was treated with VISINE. After drug was administered, patient experienced the following problems/side effects: application site reaction, eye irritation, eye swelling, ocular hyperaemia, vision blurred, . VISINE dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Metvix Side Effects Report #5526121-8
Consumer or non-health professional from GERMANY reported METVIX problem on Nov 05, 2007. Male patient, 68 years of age, was diagnosed with actinic keratosis and was treated with METVIX. After drug was administered, patient experienced the following problems/side effects: application site reaction, blood glucose increased, chills, malaise, pain in extremity, pyrexia, skin reaction, . METVIX dosage: unknown. Patient recovered.
APPLICATION SITE REACTION : Estraderm Side Effects Report #5526605-2
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 23, 2007. Female patient, 26 years of age, weighting 116.8 lb, was diagnosed with ovarian failure, osteoporosis, eczema, depression and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: application site reaction, nausea, night sweats, pain, . ESTRADERM dosage: unknown. During the same period patient was treated with BONIVA, ACRIVASTINE, CITALOPRAM. Patient recovered.
APPLICATION SITE REACTION : Xalatan Side Effects Report #5491020-7
Physician from PORTUGAL reported XALATAN problem on Oct 10, 2007. Male patient, 70 years of age, was diagnosed with glaucoma and was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: application site reaction, keratitis, . XALATAN dosage: unknown. Patient recovered.