ACARODERMATITIS side effect
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Drugs associated with ACARODERMATITIS
AVONEX BARACLUDE BEXXAR CHANTIX CIPROFLOXACIN FACTIVE FOSAMAX HUMIRA KETEK MICARDIS NEORAL ORTHO SPIRIVA TAGAMET TEMODAL VYTORIN ZYBANBexxar Side Effects Report #5583114-2
Consumer or non-health professional from UNITED STATES reported BEXXAR problem on Feb 20, 2007. Female patient, 48 years of age, weighting 133.4 lb, was diagnosed with non-hodgkin's lymphoma, pruritus and was treated with BEXXAR. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, pruritus, rash, . BEXXAR dosage: unknown. During the same period patient was treated with CIMETIDINE, DICYCLOMINE, REGLAN, PHENERGAN, TOPROL, VICODIN, NASONEX. Patient recovered.
Humira Side Effects Report #5559040-1
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 17, 2007. Female patient, weighting 200.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, arthropod bite, pruritus, urticaria, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, LEVOTHYROXINE, PAROXETINE, FOLIC ACID. Patient recovered.
Tagamet Side Effects Report #5482397-7
Consumer or non-health professional from JAPAN reported TAGAMET problem on Oct 09, 2007. Female patient, 83 years of age, was diagnosed with gastritis, hypertension and was treated with TAGAMET. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, blood potassium increased, disseminated intravascular coagulation, pruritus, rash, rash papular, skin erosion, tongue ulceration, toxic epidermal necrolysis, . TAGAMET dosage: unknown. During the same period patient was treated with PREDNISOLONE, NORVASC, BASEN, BAKTAR. Patient died.
Temodal Side Effects Report #5451914-5
TEMODAL problem was reported by a Physician from JAPAN on Sept 06, 2007. Male patient, 80 years of age, weighting 85.98 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, disseminated intravascular coagulation, guttate psoriasis, neutrophil count increased, platelet count decreased, pneumonia aspiration, renal impairment, urinary retention, . TEMODAL dosage: unknown. During the same period patient was treated with PREDONINE, BASEN, STARSIS, PARULEON, MAGNESIUM OXIDE, DEPAS. Patient recovered.
Bexxar Side Effects Report #5418027-X
Consumer or non-health professional from UNITED STATES reported BEXXAR problem on Feb 20, 2007. Female patient, 48 years of age, weighting 133.4 lb, was diagnosed with non-hodgkin's lymphoma, pruritus and was treated with BEXXAR. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, pruritus, rash, . BEXXAR dosage: unknown. During the same period patient was treated with CIMETIDINE, DICYCLOMINE, REGLAN, PHENERGAN, TOPROL, VICODIN, NASONEX. Patient recovered.
Ortho Side Effects Report #5425104-6
ORTHO EVRA problem was reported by a Physician from BRAZIL on Aug 20, 2007. Female patient, weighting 119.0 lb, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, syncope, . ORTHO EVRA dosage: unknown. Patient recovered.
Micardis Side Effects Report #5429958-9
Consumer or non-health professional from UNITED STATES reported MICARDIS problem on Aug 29, 2007. Female patient, 77 years of age, was diagnosed with hypertension, vitamin supplementation and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, . MICARDIS dosage: unknown. During the same period patient was treated with PROTONIX, PRESER VISION. Patient recovered.
Factive Side Effects Report #5403393-1
FACTIVE problem was reported by a Physician from JORDAN on July 13, 2007. Female patient, 25 years of age, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, . FACTIVE dosage: 320 MG, QD. Patient was hospitalized. Patient recovered.
Factive Side Effects Report #5403393-1
Physician from JORDAN reported FACTIVE problem on July 13, 2007. Female patient, 25 years of age, was diagnosed with bronchitis and was treated with FACTIVE. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, . FACTIVE dosage: 320 MG, QD. Patient was hospitalized. Patient recovered.
Neoral Side Effects Report #5763607-5
NEORAL problem was reported by a Health Professional from on June 04, 2008. Male patient was diagnosed with pemphigoid and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, septic shock, . NEORAL dosage: 200 MG/DAY. During the same period patient was treated with PREDONINE, WARFARIN, LECTISOL, DERMOVATE. Patient was hospitalized. Patient died on 04/01/2006.
Neoral Side Effects Report #5774346-9
Health Professional from reported NEORAL problem on June 12, 2008. Male patient was diagnosed with pemphigoid and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, blister, pyrexia, septic shock, skin exfoliation, . NEORAL dosage: 200 MG/DAY. During the same period patient was treated with PREDONINE, WARFARIN, LECTISOL, DERMOVATE. Patient was hospitalized. Patient died on 04/01/2006.
Fosamax Side Effects Report #5776027-4
FOSAMAX problem was reported by a Physician from UNITED STATES on June 12, 2008. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, alcohol abuse, hyperkeratosis, hypoglycaemia, microcytosis, osteomyelitis, osteonecrosis, upper limb fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with INDERAL, DETROL. Patient was hospitalized. Patient recovered.
Ketek Side Effects Report #5781808-7
Consumer or non-health professional from UNITED STATES reported KETEK problem on June 12, 2008. Female patient was diagnosed with influenza, respiratory tract infection and was treated with KETEK. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, actinic keratosis, diarrhoea, eczema, impetigo, keratoacanthoma, neurodermatitis, prurigo, pruritus, . KETEK dosage: DOSE: ^400 MG INCREMENTS^. During the same period patient was treated with CHLORASEPTIC, XOPONEX. Patient recovered.
Ciprofloxacin Side Effects Report #5789181-5
CIPROFLOXACIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 16, 2008. Female patient, 17 years of age, was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, blister, rash, . CIPROFLOXACIN dosage: unknown. Patient recovered.
Zyban Side Effects Report #5736392-0
Consumer or non-health professional from CANADA reported ZYBAN problem on May 06, 2008. Male patient, 41 years of age, weighting 251.5 lb, was diagnosed with anxiety and was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, anger, anorexia, anxiety, blood iron increased, bursitis, constipation, decreased appetite, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with VALIUM. Patient recovered.
Ketek Side Effects Report #5742671-3
KETEK problem was reported by a Consumer or non-health professional from UNITED STATES on May 12, 2008. Female patient was treated with KETEK. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, actinic keratosis, eczema, impetigo, neurodermatitis, pruritus, rash, skin bacterial infection, squamous cell carcinoma, . KETEK dosage: DOSE: ^400 MG INCREMENTS^. Patient recovered.
Chantix Side Effects Report #5754317-9
Physician from UNITED STATES reported CHANTIX problem on May 19, 2008. Female patient, weighting 130.1 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, diplopia, dizziness, erythema, eye disorder, hypertension, impaired driving ability, . CHANTIX dosage: unknown. Patient recovered.
Baraclude Side Effects Report #5372312-9
BARACLUDE problem was reported by a Physician from UNITED STATES on Apr 06, 2007. Male patient, 23 years of age, was treated with BARACLUDE. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, dermatitis contact, . BARACLUDE dosage: unknown. Patient recovered.
Avonex Side Effects Report #5375734-5
Health Professional from UNITED STATES reported AVONEX problem on June 21, 2007. Male patient, 45 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, depression, fall, impaired healing, skin ulcer, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Vytorin Side Effects Report #5355990-X
VYTORIN problem was reported by a Health Professional from UNITED STATES on Jan 31, 2007. Female patient was diagnosed with blood cholesterol increased, hyperlipidaemia and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, pruritus, . VYTORIN dosage: 10-20 MG/DAILY/PO. During the same period patient was treated with COUMADIN, MAXZIDE, REMERON, ATENOLOL. Patient recovered.
Spiriva Side Effects Report #5273159-4
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Mar 20, 2007. Male patient, weighting 149.9 lb, was diagnosed with chronic obstructive pulmonary disease, emphysema, hypertension, anxiety and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: acarodermatitis, accidental exposure, acute respiratory failure, anxiety, aspiration, bronchitis, chronic obstructive pulmonary disease, condition aggravated, constipation, . SPIRIVA dosage: unknown. During the same period patient was treated with DUONEB, ADVAIR DISKUS, HYDROCHLOROTHIAZIDE, XANAX, ALBUTEROL RESCUE INHALER, OXYGEN, FLOMAX. Patient was hospitalized. Patient recovered.