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APPLICATION SITE HYPERSENSITIVITY side effect

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Humira Side Effects Report #5673685-X
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Mar 14, 2008. Female patient, 24 years of age, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: application site hypersensitivity, knee arthroplasty, . HUMIRA dosage: unknown. During the same period patient was treated with INSULIN, METHOTREXATE, LEFLUNOMIDE, TOENOL, MELOXICAM, ALENDRONATE, VITAMIN B, CALCIUM. Patient recovered.

Neupro Side Effects Report #5679921-8
NEUPRO problem was reported by a Physician from GERMANY on Mar 07, 2008. Female patient, 73 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 hypersensitivity, dermatitis contact, . NEUPRO dosage: 8MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Catapres Side Effects Report #5506981-7
Physician from reported CATAPRES problem on Oct 12, 2007. Female patient, 93 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 hypersensitivity, application site pruritus, blood pressure increased, . CATAPRES dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, HYDROCORTISONE, ANTIVERT. Patient recovered.

Proactive Side Effects Report #5397590-1
PROACTIVE problem was reported by a Consumer or non-health professional from UNITED STATES on July 23, 2007. Female patient, 28 years of age, weighting 200.0 lb, was diagnosed with acne and was treated with PROACTIVE. After drug was administered, patient experienced the following problems/side effects: application site hypersensitivity, erythema, pruritus, . PROACTIVE dosage: unknown. Patient recovered.


Proactive Side Effects Report #5397590-1
Consumer or non-health professional from UNITED STATES reported PROACTIVE problem on July 23, 2007. Female patient, 28 years of age, weighting 200.0 lb, was diagnosed with acne and was treated with PROACTIVE. After drug was administered, patient experienced the following problems/side effects: application site hypersensitivity, erythema, pruritus, . PROACTIVE dosage: unknown. Patient recovered.

Ortho Side Effects Report #5793478-2
ORTHO EVRA problem was reported by a Consumer or non-health professional from BRAZIL on June 17, 2008. Female patient, 29 years of age, was diagnosed with contraception and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: application site hypersensitivity, cyst, haemorrhagic cyst, superovulation, . ORTHO EVRA dosage: unknown. During the same period patient was treated with ORTHO EVRA. Patient was hospitalized. Patient recovered.

Benzoin Side Effects Report #5742454-4
Pharmacist from UNITED STATES reported BENZOIN COMPOUND problem on May 14, 2008. Male patient, 56 years of age, weighting 94.20 lb, was diagnosed with surgery and was treated with BENZOIN COMPOUND. After drug was administered, patient experienced the following problems/side effects: application site hypersensitivity, erythema multiforme, . BENZOIN COMPOUND dosage: unknown. Patient was hospitalized. Patient recovered.

Preparation Side Effects Report #5691203-7
PREPARATION H COOLING problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 25, 2008. Male patient, 37 years of age, weighting 244.2 lb, was diagnosed with haemorrhoids and was treated with PREPARATION H COOLING. After drug was administered, patient experienced the following problems/side effects: application site hypersensitivity, application site irritation, application site pruritus, application site rash, . PREPARATION H COOLING dosage: unknown. Patient recovered.

Combipatch Side Effects Report #5297902-3
Consumer or non-health professional from UNITED STATES reported COMBIPATCH problem on Apr 03, 2007. Female patient, 64 years of age, weighting 192.0 lb, was diagnosed with menopause and was treated with COMBIPATCH. After drug was administered, patient experienced the following problems/side effects: application site hypersensitivity, blood triglycerides increased, breast cancer stage i, breast cyst, breast microcalcification, cataract, cataract operation, cervical dysplasia, colitis ischaemic, . COMBIPATCH dosage: unknown. During the same period patient was treated with CLIMARA, PREMARIN, PROVERA. Patient was hospitalized. Patient recovered.


Neosporin Side Effects Report #5773061-5
NEOSPORIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 30, 2008. Female patient, 52 years of age, weighting 180.0 lb, was diagnosed with surgery and was treated with NEOSPORIN. After drug was administered, patient experienced the following problems/side effects: application site burn, application site exfoliation, application site hypersensitivity, application site oedema, application site pain, infection, oedema mouth, rash, . NEOSPORIN dosage: unknown. During the same period patient was treated with PREDNISONE, DIPHENHYDRAMINE. Patient recovered.