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APPLICATION SITE INFECTION side effect

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Climara Side Effects Report #5637995-4
Consumer or non-health professional from UNITED STATES reported CLIMARA PRO problem on Jan 23, 2008. Female patient, 51 years of age, weighting 132.3 lb, was treated with CLIMARA PRO. After drug was administered, patient experienced the following problems/side effects: application site infection, application site pruritus, application site rash, . CLIMARA PRO dosage: unknown. Patient recovered.

Avastin Side Effects Report #5584574-3
AVASTIN problem was reported by a Physician from UNITED STATES on Dec 31, 2007. Female patient, 76 years of age, was diagnosed with colorectal cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: application site infection, wound dehiscence, . AVASTIN dosage: 5 MG/KG, UNK. During the same period patient was treated with CAMPTOSAR, FLUOROURACIL, LEUCOVORIN. Patient died on 09/20/2007.

Aldara Side Effects Report #5586460-1
Consumer or non-health professional from UNITED STATES reported ALDARA problem on Jan 08, 2008. Female patient, 37 years of age, weighting 120.0 lb, was diagnosed with basal cell carcinoma and was treated with ALDARA. After drug was administered, patient experienced the following problems/side effects: application site infection, crying, lymphadenopathy, . ALDARA dosage: unknown. Patient recovered.

Protopic Side Effects Report #5483242-6
PROTOPIC problem was reported by a Physician from JAPAN on Sept 25, 2007. Male patient, 13 years of age, was treated with PROTOPIC. After drug was administered, patient experienced the following problems/side effects: application site infection, application site warmth, kaposi's varicelliform eruption, . PROTOPIC dosage: unknown. During the same period patient was treated with PALDES, VOALLA, WHITE PETROLEUM, HIRUDOID, ALLEGRA, LIDOMEX, DIFLUPREDNATE, ANTEBATE. Patient was hospitalized. Patient recovered.


Abreva Side Effects Report #5461349-7
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Sept 21, 2006. Male patient, child 4 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, application site pain, lip haemorrhage, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461837-3
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 29, 2006. Female patient, 26 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, hypersensitivity, lip swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462169-X
Consumer or non-health professional from UNITED STATES reported ABREVA problem on May 15, 2007. Female patient, 33 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, oral herpes, pallor, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462237-2
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 25 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, application site scar, application site swelling, hypersensitivity, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462518-2
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Jan 25, 2007. Female patient, 31 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, oral herpes, . ABREVA dosage: unknown. Patient recovered.


Abreva Side Effects Report #5462523-6
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 26, 2007. Female patient, 22 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462539-X
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Jan 30, 2007. Female patient, 61 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, application site pain, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462727-2
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 01, 2007. Female patient, child 11 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, application site scab, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462830-7
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Mar 22, 2007. Female patient, 21 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site infection, hypersensitivity, lip swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Duragesic Side Effects Report #5360021-1
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on June 07, 2007. Male patient, weighting 200.0 lb, was diagnosed with pain, neuralgia, anxiety and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site infection, back pain, catheter site haemorrhage, catheter site infection, diplegia, inadequate analgesia, neuralgia, open wound, stomach discomfort, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, NEURONTIN, VALIUM, XANAX, OXYCODONE. Patient was hospitalized. Patient recovered.


Byetta Side Effects Report #5493511-1
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Oct 11, 2007. Male patient, weighting 261.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: allergy to vaccine, application site infection, application site mass, application site rash, blood pressure decreased, hyperhidrosis, pallor, pyrexia, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, INFLUENZA VACCINE, PNEUMOCOCCAL VACCINE. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5746609-4
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on May 12, 2008. Female patient, weighting 155.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: application site excoriation, application site infection, application site irritation, application site vesicles, feeling abnormal, spinal fracture, . DURAGESIC dosage: unknown. During the same period patient was treated with OXYCONTIN, VICODIN. Patient was hospitalized. Patient recovered.

Fragmin Side Effects Report #5712648-2
Pharmacist from BRAZIL reported FRAGMIN problem on Apr 07, 2008. Female patient, 40 years of age, was diagnosed with prophylaxis of abortion and was treated with FRAGMIN. After drug was administered, patient experienced the following problems/side effects: application site discomfort, application site infection, . FRAGMIN dosage: unknown. Patient recovered.

Duragesic Side Effects Report #5259610-4
DURAGESIC problem was reported by a Physician from UNITED STATES on Feb 28, 2007. Female patient, 53 years of age, weighting 130.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: anxiety, application site infection, application site pruritus, application site vesicles, dehydration, dermatitis contact, diarrhoea, disturbance in attention, . DURAGESIC dosage: unknown. During the same period patient was treated with FENAGRIN SUPPOSITORY. Patient recovered.