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APPLICATION SITE REACTION side effect

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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.

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.

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.

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.


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.

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.

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.

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.

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.


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.

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.

Voltaren Side Effects Report #5597154-0
VOLTAREN problem was reported by a Consumer or non-health professional from FRANCE 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.

Neupro Side Effects Report #5610421-7
Consumer or non-health professional from UNITED STATES reported NEUPRO problem 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.

Kentera Side Effects Report #5614864-7
KENTERA problem was reported by a Health Professional from UNITED KINGDOM 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.


Zovirax Side Effects Report #5535708-8
Consumer or non-health professional from UNITED STATES reported ZOVIRAX problem 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.

Duragesic Side Effects Report #5537002-8
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Fentanyl Side Effects Report #5537710-9
Consumer or non-health professional from UNITED STATES reported FENTANYL problem 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.

Emsam Side Effects Report #5546027-8
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Emsam Side Effects Report #5546029-1
Consumer or non-health professional from UNITED STATES reported EMSAM problem 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.


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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Nitro Side Effects Report #5582842-2
NITRO problem was reported by a Physician from ITALY 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.

Neupro Side Effects Report #5587795-9
Physician from UNITED STATES reported NEUPRO problem 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.

Neupro Side Effects Report #5587865-5
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Neupro Side Effects Report #5588944-9
Consumer or non-health professional from UNITED STATES reported NEUPRO problem 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.

Neupro Side Effects Report #5588946-2
NEUPRO problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Neupro Side Effects Report #5588954-1
Consumer or non-health professional from UNITED STATES reported NEUPRO problem 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.

Gold Side Effects Report #5507239-2
GOLD BOND HEALING MEDICATED BODY problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Estraderm Side Effects Report #5511150-0
Consumer or non-health professional from UNITED KINGDOM reported ESTRADERM problem 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.

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.

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.

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.

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.

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.

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.

Catapres Side Effects Report #5495097-4
CATAPRES problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient, 70 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 reaction, . CATAPRES dosage: unknown. Patient recovered.

Fentanyl Side Effects Report #5441449-8
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Aug 23, 2007. Male patient, weighting 320.0 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 reaction, dizziness, euphoric mood, hypoaesthesia, intervertebral disc protrusion, nausea, oedema peripheral, . 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, PERCOCET. Patient recovered.

Emsam Side Effects Report #5448764-2
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on June 05, 2007. Female patient, 57 years of age, weighting 114.6 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 XANAX, ESTROGEN, KLONOPIN, VAGIFEM. Patient recovered.

Emsam Side Effects Report #5448768-X
Consumer or non-health professional from UNITED STATES reported EMSAM problem on June 21, 2007. Female patient, 27 years of age, 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 DOXYCYCLINE. Patient recovered.

Emsam Side Effects Report #5448770-8
EMSAM problem was reported by a Physician from UNITED STATES on July 23, 2007. Female patient, 35 years of age, 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 LITHIUM CARBONATE, SEROQUEL, ABILIFY, SYNTHROID. Patient recovered.

Emsam Side Effects Report #5448781-2
Consumer or non-health professional from UNITED STATES reported EMSAM problem on June 08, 2007. Female patient, 62 years of age, weighting 108.0 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: EMSAM 6MG/24HOURS PATCH FOR 12 HOURS/DAY INSTEAD OF 24 HOURS. During the same period patient was treated with VALIUM. Patient recovered.

Emsam Side Effects Report #5448786-1
EMSAM problem was reported by a Consumer or non-health professional from UNITED STATES on June 12, 2007. Female patient, weighting 145.5 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 KLONOPIN, SEROQUEL, ENCORTON. Patient recovered.

Emsam Side Effects Report #5448790-3
Consumer or non-health professional from UNITED STATES reported EMSAM problem on June 13, 2007. Male patient, weighting 229.3 lb, was diagnosed with depression, panic attack, 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 INDERAL, ZESTRIL, LAMICTAL, LITHIUM CARBONATE, XANAX, SYNTHROID. Patient recovered.