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INJECTION SITE BRUISING side effect

What is INJECTION SITE BRUISING ?
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Drugs associated with INJECTION SITE BRUISING

APIDRA  APLISOL  APOKYN  APTIVUS  ARANESP  ARIXTRA  AVANDIA  AVONEX  BETASERON  BONIVA  BOTOX  BYETTA  ENBREL  ENOXAPARIN  EPINEPHRINE  EPIPEN  EPOGEN  EXENATIDE  FORTEO  FUZEON  HEPARIN  HUMATROPE  HUMIRA  HUMULIN  IMITREX  INCRELEX  LANTUS  LEVEMIR  LOVENOX  NUTROPIN  PLAVIX  PROCRIT  REBIF  SAIZEN  SEROQUEL  SYMLIN  TUBERSOL  ZEMPLAR  


Humira Side Effects Report #5665418-8
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Dec 06, 2007. Female patient, weighting 160.1 lb, was diagnosed with rheumatoid arthritis, contraception and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, injection site swelling, . HUMIRA dosage: unknown. During the same period patient was treated with BIRTH CONTROL S. Patient recovered.

Humira Side Effects Report #5665431-0
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2007. Female patient, weighting 146.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5665458-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Dec 06, 2007. Female patient, weighting 135.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5666767-X
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 26, 2007. Male patient, 46 years of age, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site nodule, injection site reaction, . HUMIRA dosage: unknown. Patient recovered.


Humira Side Effects Report #5666818-2
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Dec 21, 2007. Female patient, weighting 115.1 lb, was diagnosed with rheumatoid arthritis, antiphospholipid syndrome and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . HUMIRA dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID. Patient recovered.

Humira Side Effects Report #5666939-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 07, 2008. Female patient, 54 years of age, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, ETANERCEPT. Patient recovered.

Humira Side Effects Report #5666947-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 07, 2008. Female patient, weighting 155.1 lb, was diagnosed with crohn's disease, mineral supplementation, breast cancer and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . HUMIRA dosage: unknown. During the same period patient was treated with MESALAMINE, POTASSIUM CHLORIDE, ENDOCORT, VINORELBINE TARTRATE. Patient recovered.

Humira Side Effects Report #5666949-7
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 06, 2008. Female patient, weighting 104.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site urticaria, . HUMIRA dosage: unknown. During the same period patient was treated with VITAMIN CAP, CATSCLAW. Patient recovered.

Humira Side Effects Report #5666974-6
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 04, 2008. Female patient, weighting 155.1 lb, was diagnosed with crohn's disease, mineral supplementation, hypertension, nausea, rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . HUMIRA dosage: unknown. During the same period patient was treated with CALCIUM, MOMOPRIL, PHENERGAN, FOLIC ACID. Patient recovered.


Humira Side Effects Report #5667006-6
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 08, 2008. Female patient, weighting 165.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site erythema, injection site nodule, injection site pruritus, injection site swelling, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISONE, MINOCYCLINE, ALENDRONATE. Patient recovered.

Humira Side Effects Report #5667138-2
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 11, 2008. Female patient, weighting 160.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.

Humira Side Effects Report #5667336-8
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 01, 2008. Female patient, weighting 175.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, METHOTREXATE, ESOMEPRAZOLE MAGNESIUM, NAPROXEN. Patient recovered.

Humira Side Effects Report #5667483-0
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 23, 2008. Female patient, weighting 134.1 lb, was diagnosed with rheumatoid arthritis, crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, procedural complication, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5667511-2
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 24, 2008. Female patient, weighting 180.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site reaction, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISONE. Patient recovered.


Humira Side Effects Report #5667596-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 25, 2008. Female patient, weighting 106.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site erythema, injection site reaction, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5667636-1
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site haemorrhage, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.

Humira Side Effects Report #5668030-X
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 11, 2008. Female patient, weighting 115.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5668073-6
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 13, 2008. Female patient, weighting 150.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, MELOXICAM. Patient recovered.

Humira Side Effects Report #5668152-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 14, 2008. Female patient, weighting 280.0 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . HUMIRA dosage: unknown. Patient recovered.


Humira Side Effects Report #5668189-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 18, 2008. Female patient, weighting 150.1 lb, was diagnosed with psoriasis, pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . HUMIRA dosage: unknown. During the same period patient was treated with ADVIL, FLUOXETINE HYDROCHLORIDE. Patient recovered.

Humira Side Effects Report #5668350-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 22, 2008. Female patient, weighting 165.1 lb, was diagnosed with psoriasis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, nausea, procedural complication, vomiting, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5668439-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Female patient, weighting 150.1 lb, was diagnosed with rheumatoid arthritis, hypertension, diabetes mellitus, asthma and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pruritus, . HUMIRA dosage: unknown. During the same period patient was treated with BENAZEPRIL HYDROCHLORIDE, HYDROCODONE BITARTRATE, METFORMIN, SALBUTAMOL SULPHATE, BISACODYL, GLIPIZIDE, PREDNISONE. Patient recovered.

Humira Side Effects Report #5668446-1
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 25, 2008. Male patient, weighting 210.2 lb, was diagnosed with psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site haemorrhage, . HUMIRA dosage: unknown. Patient recovered.

Humira Side Effects Report #5668497-7
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Male patient, weighting 250.2 lb, was diagnosed with psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site discolouration, injection site erythema, injection site inflammation, injection site nodule, injection site swelling, . HUMIRA dosage: unknown. Patient recovered.

Arixtra Side Effects Report #5615079-9
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Dec 21, 2006. Female patient, 48 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site induration, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with PROGRAF, CLONAZEPAM, WELLBUTRIN, ALDACTONE, LASIX, AMITRIPTYLINE, AMBIEN. Patient recovered.

Arixtra Side Effects Report #5615082-9
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2007. Male patient, 45 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . ARIXTRA dosage: unknown. Patient recovered.

Arixtra Side Effects Report #5615087-8
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Mar 13, 2007. Female patient, 56 years of age, weighting 223.5 lb, was diagnosed with pulmonary embolism and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site erythema, injection site haemorrhage, injection site pain, injection site swelling, . ARIXTRA dosage: 10MG PER DAY. During the same period patient was treated with COUMADIN, TYLENOL. Patient recovered.

Arixtra Side Effects Report #5615138-0
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on July 27, 2007. Female patient, 61 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site erythema, injection site swelling, injection site vesicles, . ARIXTRA dosage: unknown. During the same period patient was treated with NIFEREX, LASIX, ASPIRIN, CLONIDINE, AMIODARONE, PLAQUENIL, SYNTHROID. Patient recovered.

Arixtra Side Effects Report #5615167-7
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Oct 11, 2007. Male patient, 58 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with AMANTADINE, AMBIEN, CARBOLEVURE, REQUIP, COMTAN, ARTANE, ZYRTEC. Patient recovered.

Epipen Side Effects Report #5624045-9
EPIPEN problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 11, 2006. Female patient was treated with EPIPEN. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pallor, . EPIPEN dosage: unknown. Patient recovered.

Rebif Side Effects Report #5637656-1
Consumer or non-health professional from UNITED STATES reported REBIF problem on Feb 08, 2008. Female patient, 30 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 bruising, systemic lupus erythematosus, . REBIF dosage: unknown. Patient recovered.

Imitrex Side Effects Report #5638701-X
IMITREX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 10, 2008. Female patient, 39 years of age, was diagnosed with migraine and was treated with IMITREX. After drug was administered, patient experienced the following problems/side effects: injection site bruising, . IMITREX dosage: 6MG AS REQUIRED. During the same period patient was treated with VALIUM, DILANTIN, VICODIN. Patient recovered.

Forteo Side Effects Report #5595485-1
Consumer or non-health professional from CANADA reported FORTEO problem on Jan 07, 2008. Female patient, 93 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: injection site bruising, knee arthroplasty, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Plavix Side Effects Report #5619338-5
PLAVIX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2007. Male patient, 75 years of age, weighting 156.0 lb, was diagnosed with coronary arterial stent insertion and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, pelvic haematoma, . PLAVIX dosage: 75 MG QD - ORAL. During the same period patient was treated with LOVENOX, ASPIRIN. Patient was hospitalized. Patient recovered.

Increlex Side Effects Report #5634614-8
Consumer or non-health professional from UNITED STATES reported INCRELEX problem on Oct 25, 2007. Male patient, child 12 years of age, weighting 71.43 lb, was diagnosed with impaired fasting glucose and was treated with INCRELEX. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . INCRELEX dosage: 2.8 MG, SUBCUTANEOUS. Patient recovered.

Increlex Side Effects Report #5634926-8
INCRELEX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 21, 2007. Male patient, child 8 years of age, weighting 46.96 lb, was diagnosed with body height below normal and was treated with INCRELEX. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site haemorrhage, injection site irritation, injection site pruritus, injection site vesicles, . INCRELEX dosage: unknown. Patient recovered.

Increlex Side Effects Report #5634931-1
Consumer or non-health professional from UNITED STATES reported INCRELEX problem on Nov 27, 2007. Male patient, child 11 years of age, weighting 67.90 lb, was diagnosed with insulin-like growth factor decreased and was treated with INCRELEX. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site erythema, injection site pruritus, injection site swelling, injection site warmth, . INCRELEX dosage: unknown. Patient recovered.

Exenatide Side Effects Report #5648406-7
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 29, 2007. Female patient, 35 years of age, weighting 167.1 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site extravasation, . EXENATIDE dosage: unknown. During the same period patient was treated with EXENATIDE PEN, METFORMIN. Patient recovered.

Byetta Side Effects Report #5648582-6
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Oct 09, 2007. Female patient, 53 years of age, weighting 218.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site urticaria, overdose, pollakiuria, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE. Patient recovered.

Exenatide Side Effects Report #5649861-9
EXENATIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2007. Female patient, 64 years of age, weighting 198.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site rash, weight decreased, . EXENATIDE dosage: unknown. During the same period patient was treated with GLYBURIDE AND METFORMIN, OMEGA, INSULIN. Patient recovered.

Exenatide Side Effects Report #5649953-4
Consumer or non-health professional from UNITED STATES reported EXENATIDE problem on Dec 20, 2007. Female patient, 57 years of age, weighting 250.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with EXENATIDE. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, injection site rash, . EXENATIDE dosage: unknown. During the same period patient was treated with METFORMIN, LANTUS, PRANDIN, PREVACID, ZYRTEC. Patient recovered.

Byetta Side Effects Report #5651132-1
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 10, 2007. Female patient, 67 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site erythema, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, ACTOS. Patient recovered.

Byetta Side Effects Report #5652112-2
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Nov 19, 2007. Female patient, 72 years of age, weighting 209.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, pharyngolaryngeal pain, systemic lupus erythematosus, weight decreased, . BYETTA dosage: 5 UG, 2/D, SUBCUTANEOUS ; 10 MG, 2/D, SUBCUTANEOUS. During the same period patient was treated with AMARYL, COUMADIN, METHOTREXATE. Patient recovered.

Byetta Side Effects Report #5652616-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 28, 2007. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, rash pruritic, . BYETTA dosage: unknown. Patient recovered.

Byetta Side Effects Report #5653535-8
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Nov 09, 2007. Female patient, 56 years of age, weighting 259.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site haemorrhage, injection site irritation, injection site swelling, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE. Patient recovered.

Humatrope Side Effects Report #5537470-1
HUMATROPE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 28, 2007. Male patient, child 12 years of age, was diagnosed with growth hormone deficiency, hypothyroidism and was treated with HUMATROPE. After drug was administered, patient experienced the following problems/side effects: injection site bruising, myelodysplastic syndrome, . HUMATROPE dosage: unknown. During the same period patient was treated with SYNTHROID. Patient recovered.

Enbrel Side Effects Report #5542368-9
Physician from UNITED STATES reported ENBREL problem on Jan 03, 2007. Female patient, weighting 217.2 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site reaction, . ENBREL dosage: unknown. During the same period patient was treated with ACEBUTOLOL, ZOCOR, COZAAR, ZYRTEC, EVISTA, PRILOSEC, LUNESTA, MECLIZINE. Patient recovered.

Enbrel Side Effects Report #5552072-9
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on June 07, 2007. Female patient, weighting 177.3 lb, was diagnosed with psoriatic arthropathy, psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site erythema, injection site haemorrhage, injection site irritation, injection site nodule, injection site rash, . ENBREL dosage: unknown. Patient recovered.

Enbrel Side Effects Report #5552529-0
Physician from UNITED STATES reported ENBREL problem on June 19, 2007. Female patient, weighting 140.2 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site haemorrhage, injection site irritation, . ENBREL dosage: unknown. During the same period patient was treated with SULFASALAZINE, METHOTREXATE. Patient recovered.

Enbrel Side Effects Report #5553733-8
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on July 13, 2007. Female patient, weighting 125.7 lb, was diagnosed with juvenile arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, joint destruction, juvenile arthritis, migraine, vertigo, . ENBREL dosage: unknown. During the same period patient was treated with IBUPROFEN, MINOCIN, MISOPROSTOL, PLAQUENIL. Patient recovered.

Enbrel Side Effects Report #5556379-0
Physician from UNITED STATES reported ENBREL problem on Sept 05, 2007. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain, . ENBREL dosage: unknown. During the same period patient was treated with LEVOXYL, EFFEXOR, TEMAZEPAM, PROVIGIL. Patient recovered.

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