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INJECTION SITE NECROSIS side effect

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Lanreotide Side Effects Report #5624922-9
Physician from SWEDEN reported LANREOTIDE AUTOGEL problem on Jan 17, 2008. Female patient was diagnosed with acromegaly and was treated with LANREOTIDE AUTOGEL. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . LANREOTIDE AUTOGEL dosage: unknown. During the same period patient was treated with LERICANIDIPIN, HYDROCHLOROTHIAZIDE W. Patient was hospitalized and became disabled. Patient recovered.

Rebif Side Effects Report #5642547-6
REBIF problem was reported by a Physician from FRANCE on Feb 11, 2008. Female patient, 37 years of age, weighting 132.3 lb, was diagnosed with multiple sclerosis, back pain and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site vesicles, stevens-johnson syndrome, . REBIF dosage: unknown. During the same period patient was treated with LAMOTRIGINE. Patient recovered.

Vivitrol Side Effects Report #5660486-1
Physician from UNITED STATES reported VIVITROL problem on Nov 28, 2007. Female patient, 44 years of age, was diagnosed with alcoholism and was treated with VIVITROL. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site nodule, injection site reaction, . VIVITROL dosage: (380 MG 1X/MONTH INTRAMUSCULAR). Patient was hospitalized. Patient recovered.

Voltaren Side Effects Report #5589268-6
VOLTAREN problem was reported by a Consumer or non-health professional from BRAZIL on Jan 02, 2008. Male patient, 56 years of age, was diagnosed with scoliosis and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site rash, scab, wound, . VOLTAREN dosage: unknown. Patient recovered.


Voltaren Side Effects Report #5598103-1
Consumer or non-health professional from BRAZIL reported VOLTAREN problem on Jan 15, 2008. Male patient, 56 years of age, was diagnosed with scoliosis, hypertension and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site rash, oedema peripheral, scab, wound, . VOLTAREN dosage: unknown. During the same period patient was treated with DIGOXIN. Patient recovered.

Copaxone Side Effects Report #5633963-7
COPAXONE problem was reported by a Physician from UNITED STATES on Mar 26, 2007. Male patient, 49 years of age, was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . COPAXONE dosage: (20 MG),SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Copaxone Side Effects Report #5633973-X
Physician from UNITED STATES reported COPAXONE problem on Mar 30, 2007. Male patient, 50 years of age, was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . COPAXONE dosage: unknown. Patient was hospitalized. Patient recovered.

Copaxone Side Effects Report #5634105-4
COPAXONE problem was reported by a Physician from UNITED STATES on June 26, 2007. Female patient, 48 years of age, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . COPAXONE dosage: (20 MG),SUBCUTANEOUS. Patient recovered.

Copaxone Side Effects Report #5634148-0
Health Professional from UNITED STATES reported COPAXONE problem on Jan 03, 2007. Female patient, 30 years of age, weighting 159.0 lb, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, skin discolouration, skin ulcer, . COPAXONE dosage: (20 MG), SUBCUTANEOUS. Patient recovered.


Copaxone Side Effects Report #5634240-0
COPAXONE problem was reported by a Consumer or non-health professional from UNITED STATES on July 30, 2007. Female patient was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . COPAXONE dosage: 20 MG, SUBCUTANEOUS. Patient recovered.

Rebif Side Effects Report #5536553-X
Physician from GERMANY reported REBIF problem on Nov 19, 2007. Female patient, 18 years of age, weighting 121.3 lb, was diagnosed with encephalitis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Vivitrol Side Effects Report #5545311-1
VIVITROL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Female patient, weighting 140.0 lb, was diagnosed with alcoholism and was treated with VIVITROL. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . VIVITROL dosage: unknown. Patient recovered.

Copaxone Side Effects Report #5565909-4
Physician from CANADA reported COPAXONE problem on Nov 29, 2007. Female patient, 41 years of age, was diagnosed with multiple sclerosis and was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site pain, injection site scab, injection site scar, . COPAXONE dosage: (20 MG, ONCE A DAY) SUBCUTANEOUS. During the same period patient was treated with SYNTHROID. Patient recovered.

Rebif Side Effects Report #5512574-8
REBIF problem was reported by a Health Professional from ITALY on Oct 22, 2007. Female patient, 33 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . REBIF dosage: unknown. During the same period patient was treated with COMBINED ORAL CONTRACEPTIVE. Patient recovered.


Hydroxyzine Side Effects Report #5520513-9
Consumer or non-health professional from JAPAN reported HYDROXYZINE HYDROCHLORIDE problem on Nov 09, 2007. Male patient, weighting 129.4 lb, was treated with HYDROXYZINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . HYDROXYZINE HYDROCHLORIDE dosage: unknown. During the same period patient was treated with ATROPINE, DORAL, ADONA, TRANSAMIN. Patient recovered.

Betaseron Side Effects Report #5477638-6
BETASERON problem was reported by a Physician from UNITED STATES on Oct 03, 2007. Male patient, 66 years of age, weighting 160.0 lb, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . BETASERON dosage: unknown. Patient recovered.

Hydroxyzine Side Effects Report #5479124-6
Consumer or non-health professional from JAPAN reported HYDROXYZINE HYDROCHLORIDE problem on Sept 26, 2007. Male patient, 24 years of age, weighting 130.1 lb, was treated with HYDROXYZINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . HYDROXYZINE HYDROCHLORIDE dosage: unknown. During the same period patient was treated with ATROPINE. Patient recovered.

Methylene Side Effects Report #5504821-3
METHYLENE BLUEECTION problem was reported by a Health Professional from UNITED STATES on Sept 20, 2007. Female patient, 53 years of age, weighting 138.0 lb, was diagnosed with lymphadenopathy and was treated with METHYLENE BLUEECTION. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . METHYLENE BLUEECTION dosage: 10 ML X 1; SUBCUTANEOUS. Patient recovered.

Depocon Side Effects Report #5384595-X
Health Professional from AUSTRIA reported DEPOCON problem on July 03, 2007. Female patient, 39 years of age, weighting 149.9 lb, was diagnosed with contraception and was treated with DEPOCON. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . DEPOCON dosage: unknown. Patient recovered.


Depocon Side Effects Report #5397123-X
DEPOCON problem was reported by a Health Professional from AUSTRIA on July 16, 2007. Female patient, 39 years of age, weighting 149.9 lb, was diagnosed with contraception and was treated with DEPOCON. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . DEPOCON dosage: unknown. During the same period patient was treated with HALCION, XANOR, CIPRALEX, SEROQUEL. Patient recovered.

Betaseron Side Effects Report #5400817-0
Physician from GERMANY reported BETASERON problem on July 18, 2007. Female patient, 26 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Depocon Side Effects Report #5384595-X
DEPOCON problem was reported by a Health Professional from AUSTRIA on July 03, 2007. Female patient, 39 years of age, weighting 149.9 lb, was diagnosed with contraception and was treated with DEPOCON. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . DEPOCON dosage: unknown. Patient recovered.

Depocon Side Effects Report #5397123-X
Health Professional from AUSTRIA reported DEPOCON problem on July 16, 2007. Female patient, 39 years of age, weighting 149.9 lb, was diagnosed with contraception and was treated with DEPOCON. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . DEPOCON dosage: unknown. During the same period patient was treated with HALCION, XANOR, CIPRALEX, SEROQUEL. Patient recovered.

Betaseron Side Effects Report #5400817-0
BETASERON problem was reported by a Physician from GERMANY on July 18, 2007. Female patient, 26 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Rocephin Side Effects Report #5759957-9
Physician from FRANCE reported ROCEPHIN problem on May 26, 2008. Female patient, 70 years of age, was treated with ROCEPHIN. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, skin induration, . ROCEPHIN dosage: unknown. Patient recovered.

Atarax Side Effects Report #5793773-7
ATARAX problem was reported by a Pharmacist from JAPAN on June 24, 2008. Male patient, child 10 years of age, was treated with ATARAX. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . ATARAX dosage: unknown. During the same period patient was treated with ANAESTHETICS. Patient recovered.

Lantus Side Effects Report #5729205-4
Physician from CANADA reported LANTUS problem on Apr 30, 2008. Male patient, 26 years of age, was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site scar, . LANTUS dosage: unknown. During the same period patient was treated with HUMALOG. Patient recovered.

Lantus Side Effects Report #5730167-4
LANTUS problem was reported by a Physician from UNITED STATES on Apr 30, 2008. Female patient was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . LANTUS dosage: unknown. Patient recovered.

Somatuline Side Effects Report #5732019-2
Consumer or non-health professional from SWEDEN reported SOMATULINE AUTOGEL problem on Apr 02, 2008. Female patient, 69 years of age, was diagnosed with neuroendocrine tumour and was treated with SOMATULINE AUTOGEL. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site nodule, . SOMATULINE AUTOGEL dosage: (90 MG, EVERY 28TH DAY). Patient recovered.

Lantus Side Effects Report #5700648-8
LANTUS problem was reported by a Physician from CANADA on Apr 01, 2008. Male patient, 26 years of age, was treated with LANTUS. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site scar, . LANTUS dosage: unknown. Patient recovered.

Somatuline Side Effects Report #5705616-8
Consumer or non-health professional from SWEDEN reported SOMATULINE AUTOGEL problem on Mar 25, 2008. Female patient, 69 years of age, was treated with SOMATULINE AUTOGEL. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, injection site nodule, . SOMATULINE AUTOGEL dosage: (90 MG,) SUBCUTANEOUS. Patient recovered.

Rebif Side Effects Report #5711128-8
REBIF problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 31, 2008. Female patient was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5716007-8
Consumer or non-health professional from UNITED KINGDOM reported REBIF problem on Apr 10, 2008. Female patient, 37 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Methylprednisolo Side Effects Report #5291725-7
METHYLPREDNISOLONE ACETATE problem was reported by a Physician from UNITED KINGDOM on Apr 03, 2007. Female patient, 34 years of age, weighting 110.2 lb, was diagnosed with arthritis and was treated with METHYLPREDNISOLONE ACETATE. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, skin atrophy, . METHYLPREDNISOLONE ACETATE dosage: unknown. Patient recovered.

Rebif Side Effects Report #5315174-8
Consumer or non-health professional from NETHERLANDS reported REBIF problem on Apr 12, 2007. Female patient, 31 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site necrosis, . REBIF dosage: unknown. Patient recovered.

Diclofenac Side Effects Report #5680213-1
DICLOFENAC problem was reported by a Health Professional from TURKEY on Mar 18, 2008. Female patient, 24 years of age, was diagnosed with pubic pain and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: blood blister, injection site necrosis, musculoskeletal pain, necrotising fasciitis, pyrexia, swelling, tachycardia, . DICLOFENAC dosage: unknown. Patient was hospitalized. Patient recovered.

Betaferon Side Effects Report #5613699-9
Physician from GERMANY reported BETAFERON problem on Jan 26, 2008. Female patient, 45 years of age, was diagnosed with multiple sclerosis, folate deficiency, headache and was treated with BETAFERON. After drug was administered, patient experienced the following problems/side effects: impaired healing, injection site necrosis, injection site scab, injection site ulcer, . BETAFERON dosage: unknown. During the same period patient was treated with FOLIC ACID, TALVOSILENTE. Patient was hospitalized. Patient recovered.

Azacitidine Side Effects Report #5626358-3
AZACITIDINE problem was reported by a Physician from GERMANY on Jan 29, 2008. Male patient, 82 years of age, weighting 185.2 lb, was diagnosed with myelodysplastic syndrome and was treated with AZACITIDINE. After drug was administered, patient experienced the following problems/side effects: injection site infection, injection site necrosis, staphylococcal infection, . AZACITIDINE dosage: (75 MG/M2, DAILY X 7 DAYS), SUBCUTANEOUS. During the same period patient was treated with ALLOPURINOL, CALCIUM, ALENDRONATE, ESOMEPRAZOLE, PREDNISONE. Patient was hospitalized. Patient recovered.

Diclofenac Side Effects Report #5626886-0
Physician from TURKEY reported DICLOFENAC problem on Feb 04, 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: embolia cutis medicamentosa, injection site necrosis, injection site pain, injection site reaction, scar, skin graft, skin hypertrophy, . DICLOFENAC dosage: unknown. Patient recovered.

Betaferon Side Effects Report #5632793-X
BETAFERON problem was reported by a Health Professional from GERMANY on Feb 11, 2008. Female patient, 45 years of age, was diagnosed with multiple sclerosis, folate deficiency, headache and was treated with BETAFERON. After drug was administered, patient experienced the following problems/side effects: impaired healing, injection site necrosis, injection site scab, injection site ulcer, . BETAFERON dosage: unknown. During the same period patient was treated with FOLIC ACID, TALVOSILENTE. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5591112-8
Physician from GERMANY reported BETASERON problem on Jan 02, 2008. Female patient, 45 years of age, was diagnosed with multiple sclerosis, folate deficiency, headache and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: impaired healing, injection site necrosis, injection site scab, injection site ulcer, . BETASERON dosage: unknown. During the same period patient was treated with FOLIC ACID, TALVOSILENTE. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5613743-9
HEPARIN problem was reported by a Pharmacist from UNITED STATES on Jan 18, 2008. Female patient was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: injection site erythema, injection site necrosis, injection site pallor, injection site vesicles, skin necrosis, . HEPARIN dosage: unknown. Patient recovered.

Heparin Side Effects Report #5613744-0
Pharmacist from UNITED STATES reported HEPARIN IN problem on Jan 18, 2008. Female patient was treated with HEPARIN IN. After drug was administered, patient experienced the following problems/side effects: injection site erythema, injection site necrosis, injection site pallor, injection site vesicles, skin necrosis, . HEPARIN IN dosage: unknown. Patient recovered.

Copaxone Side Effects Report #5634116-9
COPAXONE problem was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2007. Female patient, 45 years of age, was treated with COPAXONE. After drug was administered, patient experienced the following problems/side effects: anaphylactic reaction, injection site necrosis, lymphadenopathy, throat tightness, urticaria, wound, . COPAXONE dosage: 20 MG (20 MG,1 IN 1 D) SUBCUTANEOUS. Patient recovered.

Betaseron Side Effects Report #5522641-0
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Nov 19, 2007. Female patient, 48 years of age, weighting 221.0 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: injection site infection, injection site necrosis, . BETASERON dosage: unknown. During the same period patient was treated with NEURONTIN. Patient was hospitalized. Patient recovered.

Diclofenac Side Effects Report #5526862-2
DICLOFENAC problem was reported by a Health Professional from INDIA on Nov 20, 2007. Male patient, 29 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: embolia cutis medicamentosa, injection site necrosis, injection site pain, injection site scar, injection site ulcer, injection site vesicles, . DICLOFENAC dosage: unknown. During the same period patient was treated with ANTIVENIN. Patient was hospitalized. Patient recovered.

Atarax Side Effects Report #5501065-6
Consumer or non-health professional from JAPAN reported ATARAX problem on Oct 22, 2007. Female patient, weighting 123.5 lb, was diagnosed with preoperative care and was treated with ATARAX. After drug was administered, patient experienced the following problems/side effects: injection site erythema, injection site necrosis, injection site pain, injection site swelling, oedema peripheral, skin necrosis, skin ulcer, . ATARAX dosage: unknown. During the same period patient was treated with ATROPINE SULPHATE, TALION, RIZABEN. Patient recovered.

Betaseron Side Effects Report #5385905-X
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on June 29, 2007. Male patient, 37 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: gangrene, injection site necrosis, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5389643-9
Physician from UNITED STATES reported BETASERON problem on July 03, 2007. Male patient, 60 years of age, weighting 146.0 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: decubitus ulcer, injection site necrosis, injection site ulcer, . BETASERON dosage: unknown. During the same period patient was treated with DETROL, AMANTADINE, XANAX, BUSPAR. Patient recovered.

Betaseron Side Effects Report #5400803-0
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on July 17, 2007. Female patient, 48 years of age, weighting 221.0 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: injection site infection, injection site necrosis, . BETASERON dosage: unknown. During the same period patient was treated with NEURONTIN. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5401892-X
Consumer or non-health professional from UNITED STATES reported BETASERON problem on July 18, 2007. Male patient, 37 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: gangrene, injection site necrosis, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.