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APPLICATION SITE PAIN side effect

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Campho Side Effects Report #5676934-7
Consumer or non-health professional from UNITED STATES reported CAMPHO problem on Mar 10, 2008. Female patient, 26 years of age, weighting 160.9 lb, was diagnosed with open wound, headache and was treated with CAMPHO. After drug was administered, patient experienced the following problems/side effects: application site pain, blood cholesterol increased, cervix carcinoma, diabetes mellitus, lentigo, ovarian mass, thyroid disorder, weight increased, . CAMPHO dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Altabax Side Effects Report #5619689-4
ALTABAX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2007. Male patient, 74 years of age, was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site pain, burning sensation, . ALTABAX dosage: unknown. Patient recovered.

Altabax Side Effects Report #5619690-0
Consumer or non-health professional from UNITED STATES reported ALTABAX problem on Nov 13, 2007. Female patient, 81 years of age, was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site pain, burning sensation, . ALTABAX dosage: unknown. Patient recovered.

Altabax Side Effects Report #5619744-9
ALTABAX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 17, 2007. Female patient, 18 years of age, weighting 130.3 lb, was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site pain, . ALTABAX dosage: unknown. Patient recovered.


Wart Side Effects Report #5628523-8
Physician from UNITED STATES reported WART AND MOLE VANISH PRISTINE HERBAL TOUCH problem on Feb 14, 2008. Male patient, child 11 years of age, was diagnosed with melanocytic naevus and was treated with WART AND MOLE VANISH PRISTINE HERBAL TOUCH. After drug was administered, patient experienced the following problems/side effects: application site pain, keloid scar, . WART AND MOLE VANISH PRISTINE HERBAL TOUCH dosage: unknown. Patient recovered.

Imitrex Side Effects Report #5638496-X
IMITREX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2007. Female patient, 28 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 pain, . IMITREX dosage: unknown. During the same period patient was treated with TOPAMAX. Patient recovered.

Gammagard Side Effects Report #5589582-4
Consumer or non-health professional from FRANCE reported GAMMAGARD S problem on Jan 04, 2008. Female patient, 57 years of age, was diagnosed with secondary immunodeficiency and was treated with GAMMAGARD S. After drug was administered, patient experienced the following problems/side effects: application site pain, headache, lymphangitis, phlebitis superficial, . GAMMAGARD S dosage: unknown. During the same period patient was treated with GAMMAGARD S. Patient was hospitalized. Patient recovered.

Gammagard Side Effects Report #5591355-3
GAMMAGARD S problem was reported by a Consumer or non-health professional from FRANCE on Jan 04, 2008. Female patient, 57 years of age, was diagnosed with secondary immunodeficiency and was treated with GAMMAGARD S. After drug was administered, patient experienced the following problems/side effects: application site pain, headache, lymphangitis, phlebitis superficial, . GAMMAGARD S dosage: unknown. Patient was hospitalized. Patient recovered.

Fentora Side Effects Report #5599081-1
Physician from UNITED STATES reported FENTORA problem on Jan 03, 2008. Female patient, 48 years of age, weighting 178.0 lb, was diagnosed with back pain, migraine and was treated with FENTORA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site ulcer, feeling abnormal, gingival ulceration, sedation, . FENTORA dosage: unknown. During the same period patient was treated with OXYCONTIN. Patient recovered.


Diclofenac Side Effects Report #5608903-7
DICLOFENAC problem was reported by a Health Professional from TURKEY on Jan 22, 2008. Female patient, 60 years of age, was diagnosed with back pain and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: application site pain, debridement, embolia cutis medicamentosa, skin discolouration, skin necrosis, . DICLOFENAC dosage: unknown. Patient was hospitalized. Patient recovered.

Abreva Side Effects Report #5612190-3
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Jan 31, 2008. Male patient, weighting 150.0 lb, was diagnosed with oral herpes and was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oedema mouth, swelling face, . ABREVA dosage: unknown. Patient recovered.

Gammagard Side Effects Report #5568860-9
GAMMAGARD S problem was reported by a Consumer or non-health professional from FRANCE on Dec 10, 2007. Female patient, 57 years of age, was diagnosed with secondary immunodeficiency and was treated with GAMMAGARD S. After drug was administered, patient experienced the following problems/side effects: application site pain, headache, lymphangitis, phlebitis superficial, . GAMMAGARD S dosage: unknown. During the same period patient was treated with GAMMAGARD S. Patient was hospitalized. Patient recovered.

Lantus Side Effects Report #5576974-2
Consumer or non-health professional from BRAZIL reported LANTUS problem on Dec 26, 2007. Male patient, 51 years of age, weighting 141.1 lb, was diagnosed with blood pressure and was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: application site pain, off label use, visual disturbance, . LANTUS dosage: unknown. During the same period patient was treated with OPTIPEN, VIT B, STRESS, ATENSINA. Patient recovered.

Niquitin Side Effects Report #5510675-1
NIQUITIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 02, 2007. Female patient, 40 years of age, was diagnosed with asthma and was treated with NIQUITIN. After drug was administered, patient experienced the following problems/side effects: application site pain, application site pruritus, vomiting, . NIQUITIN dosage: 21MG PER DAY. During the same period patient was treated with GABAPENTIN, SERETIDE, EVOREL. Patient recovered.


Altabax Side Effects Report #5511295-5
Consumer or non-health professional from UNITED STATES reported ALTABAX problem on Aug 02, 2007. Female patient, 60 years of age, was diagnosed with wound drainage and was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site pain, . ALTABAX dosage: unknown. During the same period patient was treated with AMBIEN, EFFEXOR, MOTRIN, FOSAMAX, HYDROCODONE BITARTRATE. Patient recovered.

Altabax Side Effects Report #5511360-2
ALTABAX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 01, 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 pain, application site ulcer, crying, . ALTABAX dosage: unknown. Patient recovered.

Altabax Side Effects Report #5511397-3
Consumer or non-health professional from UNITED STATES reported ALTABAX problem on Oct 24, 2007. Female patient, 54 years of age, was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site pain, skin discomfort, . ALTABAX dosage: 10MG TWICE PER DAY. During the same period patient was treated with TRIAMCINOLONE. Patient recovered.

Commit Side Effects Report #5517031-0
COMMIT problem was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2007. Female patient, 47 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site pain, application site pruritus, dyspepsia, hypersensitivity, malaise, stomach discomfort, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.

Commit Side Effects Report #5517307-7
Consumer or non-health professional from UNITED STATES reported COMMIT problem on Oct 11, 2007. Female patient, 52 years of age, was treated with COMMIT. After drug was administered, patient experienced the following problems/side effects: application site pain, application site urticaria, application site vesicles, cheilitis, swollen tongue, . COMMIT dosage: unknown. During the same period patient was treated with NICODERM CQ. Patient recovered.


Gammagard Side Effects Report #5518624-7
GAMMAGARD S problem was reported by a Consumer or non-health professional from FRANCE on Nov 05, 2007. Female patient, 57 years of age, was diagnosed with secondary immunodeficiency and was treated with GAMMAGARD S. After drug was administered, patient experienced the following problems/side effects: application site pain, headache, lymphangitis, phlebitis superficial, . GAMMAGARD S dosage: unknown. Patient was hospitalized. Patient recovered.

Fentora Side Effects Report #5483525-X
Consumer or non-health professional from UNITED STATES reported FENTORA problem on July 31, 2007. Female patient, 48 years of age, weighting 178.0 lb, was diagnosed with back pain, migraine and was treated with FENTORA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site ulcer, gingival ulceration, incorrect dose administered, mouth ulceration, somnolence, tongue haemorrhage, tongue ulceration, . FENTORA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461162-0
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 26, 2006. Female patient, 58 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site swelling, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461165-6
Consumer or non-health professional from UNITED STATES reported ABREVA problem on July 27, 2006. Female patient, 37 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461321-7
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2006. Female patient, 22 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461445-4
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Oct 16, 2006. Female patient, 30 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5461847-6
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 29, 2006. Female patient, 58 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462079-8
Consumer or non-health professional from UNITED STATES reported ABREVA problem on May 01, 2007. Male patient, child 7 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462122-6
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on May 03, 2007. Male patient, 60 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462224-4
Consumer or non-health professional from UNITED STATES reported ABREVA problem on May 30, 2007. Female patient, 28 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site paraesthesia, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462321-3
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on June 25, 2007. Male patient, 61 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site pruritus, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462377-8
Consumer or non-health professional from UNITED STATES reported ABREVA problem on July 10, 2007. Female patient, 72 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462509-1
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 24, 2007. Female patient, 16 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462532-7
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Jan 29, 2007. Female patient, 66 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462569-8
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 02, 2007. Male patient, 36 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462584-4
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Feb 06, 2007. Female patient, 24 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, application site swelling, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462708-9
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 27, 2007. Female patient, 50 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462764-8
Consumer or non-health professional from UNITED STATES reported ABREVA problem on Mar 12, 2007. Female patient, 34 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Abreva Side Effects Report #5462850-2
ABREVA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 27, 2007. Female patient, 37 years of age, was treated with ABREVA. After drug was administered, patient experienced the following problems/side effects: application site pain, oral herpes, . ABREVA dosage: unknown. Patient recovered.

Altabax Side Effects Report #5419347-5
Consumer or non-health professional from UNITED STATES reported ALTABAX problem on Aug 15, 2007. Female patient, 71 years of age, weighting 134.0 lb, was diagnosed with infection prophylaxis and was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site pain, open wound, . ALTABAX dosage: unknown. Patient recovered.

Aldara Side Effects Report #5402429-1
ALDARA problem was reported by a Health Professional from UNITED STATES on July 30, 2007. Female patient, 46 years of age, weighting 128.0 lb, was diagnosed with anogenital warts and was treated with ALDARA. After drug was administered, patient experienced the following problems/side effects: application site pain, burning sensation, erythema, genital pain, swelling, . ALDARA dosage: unknown. Patient recovered.

Aldara Side Effects Report #5402429-1
Health Professional from UNITED STATES reported ALDARA problem on July 30, 2007. Female patient, 46 years of age, weighting 128.0 lb, was diagnosed with anogenital warts and was treated with ALDARA. After drug was administered, patient experienced the following problems/side effects: application site pain, burning sensation, erythema, genital pain, swelling, . ALDARA dosage: unknown. Patient recovered.

Zoladex Side Effects Report #5757101-5
ZOLADEX problem was reported by a Consumer or non-health professional from BRAZIL on May 26, 2008. Female patient, 48 years of age, weighting 138.9 lb, was diagnosed with leiomyoma and was treated with ZOLADEX. After drug was administered, patient experienced the following problems/side effects: application site pain, blood pressure decreased, chromaturia, headache, nausea, pyrexia, rash, urine odour abnormal, weight decreased, . ZOLADEX dosage: unknown. Patient recovered.

Neupro Side Effects Report #5732589-4
Consumer or non-health professional from UNITED STATES reported NEUPRO problem on Apr 21, 2008. Female patient, 71 years of age, weighting 108.0 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 pain, gait disturbance, middle insomnia, psychomotor hyperactivity, somnolence, tremor, . NEUPRO dosage: unknown. During the same period patient was treated with CARBIDOPA AND LEVODOPA. Patient recovered.

Altabax Side Effects Report #5733696-2
ALTABAX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 29, 2008. Female patient, 85 years of age, was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site pain, erythema, skin injury, skin irritation, . ALTABAX dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE, PREVACID. Patient recovered.

Climara Side Effects Report #5698742-3
Consumer or non-health professional from UNITED STATES reported CLIMARA problem on Apr 25, 2007. Female patient, 39 years of age, weighting 180.8 lb, was diagnosed with menopausal symptoms prophylaxis and was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: application site pain, . CLIMARA dosage: unknown. During the same period patient was treated with SYNTHROID. Patient recovered.

Campho Side Effects Report #5700072-8
CAMPHO problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 04, 2008. Female patient, 26 years of age, weighting 160.9 lb, was diagnosed with open wound, headache and was treated with CAMPHO. After drug was administered, patient experienced the following problems/side effects: application site pain, blood cholesterol increased, cervix carcinoma, diabetes mellitus, lentigo, ovarian mass, thyroid disorder, weight increased, . CAMPHO dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Niquitin Side Effects Report #5316993-4
Consumer or non-health professional from UNITED KINGDOM reported NIQUITIN problem on Apr 27, 2007. Female patient, 28 years of age, was treated with NIQUITIN. After drug was administered, patient experienced the following problems/side effects: application site pain, application site pruritus, chest pain, dizziness, fatigue, feeling hot, . NIQUITIN dosage: 21MG SINGLE DOSE. Patient recovered.

Fentanyl Side Effects Report #5339822-1
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Physician from UNITED STATES on May 21, 2007. Female patient, weighting 138.0 lb, was diagnosed with pain, back pain, depression, multiple allergies, asthma, laxative supportive care and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pain, application site vesicles, migraine, spinal disorder, therapeutic response decreased, weight decreased, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with DURAGESIC, PERCOCET, PAXIL CR, ALLEGRA, SINGULAIR, ADVAIR DISKUS, ALBUTEROL, GLYCOLAX. Patient recovered.

Ceftriaxone Side Effects Report #5341416-9
Consumer or non-health professional from BRAZIL reported CEFTRIAXONE problem on May 16, 2007. Male patient, child 6 years of age, weighting 55.12 lb, was diagnosed with urinary tract infection and was treated with CEFTRIAXONE. After drug was administered, patient experienced the following problems/side effects: application site pain, syncope, . CEFTRIAXONE dosage: 1000 MG, QD, INTRAVENOUS. Patient recovered.

Niquitin Side Effects Report #5286741-5
NIQUITIN CQ PATCH problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 27, 2007. Female patient, 28 years of age, was treated with NIQUITIN CQ PATCH. After drug was administered, patient experienced the following problems/side effects: application site pain, chest pain, dizziness, fatigue, feeling hot, pain in extremity, pruritus, . NIQUITIN CQ PATCH dosage: 21MG PER DAY. Patient recovered.

Fentanyl Side Effects Report #5256091-1
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 26, 2007. Female patient, weighting 125.0 lb, was diagnosed with pain, back pain, depression, multiple allergies, asthma, laxative supportive care and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: application site pain, application site vesicles, migraine, spinal disorder, therapeutic response decreased, weight decreased, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with DURAGESIC, PERCOCET, PAXIL CR, ALLEGRA, ADVAIR DISKUS, ALBUTEROL, GLYCOLAX. Patient recovered.