INJECTION SITE REACTION side effect
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Drugs associated with INJECTION SITE REACTION
ALDURAZYME APTIVUS ARANESP AUGMENTIN AVANDIA AVASTIN AVELOX AVONEX BENEFIX BETAFERON BETASERON BONIVA BUPRENORPHINE BYETTA CAMPATH CARDIOLITE CEREBYX CETUXIMAB CIPROFLOXACINECT CLADRIBINE COPAXONE CYCLOPHOSPHAMIDE DEPO DIPYRIDAMOLE DOXYCYCLINE ENANTONE ENBREL ENOXAPARIN EPINEPHRINE EPIPEN ERAXIS ETHYOL FASLODEX FORTEO FRAGMIN FUZEON HANCE HEPARIN HUMIRA INCRELEX ISENTRESS ISOVUE JUVEDERM KENALOG KINERET LEUPROLIDE LEVAQUIN LEVEMIR LEVOFLOXACIN LIDOCAINE LOVENOX MABCAMPATH METHOTREXATE MIDAZOLAM NEULASTA NOVORAPID ONCASPAR PROCALAMINE PROCRIT RAPTIVA REBIF RITUXAN SUBUTEX TAVANIC TAXOL TORADOL TUBERSOL TUBERTEST ULTRAVIST VANCOMYCIN VAPRISOL VENOFER VIRAFERONPEG VIVITROL VYTORIN XOLAIR ZOLOFTRebif Side Effects Report #5658019-9
Consumer or non-health professional from UNITED STATES reported REBIF problem on Feb 25, 2008. Female patient, 34 years of age, weighting 120.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site reaction, ovarian cyst, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5662767-4
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on Mar 06, 2008. Male patient, 54 years of age, was diagnosed with ankylosing spondylitis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, swelling face, urticaria, . HUMIRA dosage: unknown. During the same period patient was treated with BENDROFLUMETHIAZIDE. Patient recovered.
Humira Side Effects Report #5666450-0
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Dec 14, 2007. Male patient, weighting 120.1 lb, was diagnosed with crohn's disease, rheumatoid arthritis, colitis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . HUMIRA dosage: unknown. During the same period patient was treated with MERCAPTOPURINE. Patient recovered.
Humira Side Effects Report #5667131-X
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 10, 2008. Female patient, 32 years of age, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . HUMIRA dosage: unknown. Patient recovered.
Humira Side Effects Report #5667513-6
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 23, 2008. Male patient, weighting 169.2 lb, was diagnosed with psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, pruritus, . HUMIRA dosage: unknown. Patient recovered.
Humira Side Effects Report #5668010-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 22, 2008. Female patient, weighting 157.1 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 reaction, pain, pruritus, swelling, . HUMIRA dosage: unknown. Patient recovered.
Humira Side Effects Report #5668075-X
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 13, 2008. Male patient, weighting 215.4 lb, was diagnosed with crohn's disease, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, rash pruritic, . HUMIRA dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, VALACYCLOVIR. Patient recovered.
Humira Side Effects Report #5668394-7
HUMIRA problem was reported by a Health Professional from UNITED STATES on Feb 25, 2008. Female patient, 21 years of age, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, injection site urticaria, . HUMIRA dosage: unknown. Patient recovered.
Humira Side Effects Report #5668410-2
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 26, 2008. Female patient, weighting 170.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . HUMIRA dosage: unknown. Patient recovered.
Fuzeon Side Effects Report #5613951-7
FUZEON problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 24, 2008. Male patient, 46 years of age, weighting 160.1 lb, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: injection site reaction, lipodystrophy acquired, . FUZEON dosage: unknown. During the same period patient was treated with PREZISTA, TRUVADA, ZIAGEN, NORVIR. Patient recovered.
Rebif Side Effects Report #5631536-3
Consumer or non-health professional from UNITED STATES reported REBIF problem on Feb 05, 2008. Female patient, 34 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 reaction, ovarian cyst, . REBIF dosage: unknown. Patient recovered.
Kenalog Side Effects Report #5637224-1
KENALOG problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 10, 2007. Female patient, 17 years of age, weighting 99.21 lb, was diagnosed with monarthritis and was treated with KENALOG. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . KENALOG dosage: unknown. During the same period patient was treated with CEFZIL, PROMETHAZINE, VIRAVAN. Patient recovered.
Heparin Side Effects Report #5639156-1
Consumer or non-health professional from UNITED STATES reported HEPARIN problem on Feb 19, 2008. Female patient, 56 years of age, weighting 132.3 lb, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: injection site reaction, urticaria, . HEPARIN dosage: unknown. During the same period patient was treated with TRANCODOL, SYNTHROID, CALCITRIOL. Patient recovered.
Heparin Side Effects Report #5640380-2
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2008. Female patient, 56 years of age, weighting 132.3 lb, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: injection site reaction, urticaria, . HEPARIN dosage: unknown. During the same period patient was treated with TRANCODOL, SYNTHROID, CALCITRIOL. Patient recovered.
Toradol Side Effects Report #5609202-X
Physician from UNITED STATES reported TORADOL problem on Jan 30, 2008. Female patient, weighting 212.0 lb, was diagnosed with back pain and was treated with TORADOL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, pyomyositis, . TORADOL dosage: 60MG ONE TIME IM. During the same period patient was treated with GABAPENTIN, INSULIN SQ. Patient was hospitalized. Patient recovered.
Kineret Side Effects Report #5609438-8
KINERET problem was reported by a Consumer or non-health professional from SWITZERLAND on Jan 16, 2008. Female patient, weighting 136.7 lb, was treated with KINERET. After drug was administered, patient experienced the following problems/side effects: injection site reaction, urinary tract infection, . KINERET dosage: unknown. During the same period patient was treated with GLIBENCLAMIDE, METFORMIN, ASPIRIN, CALCIUM GLUCONATE, LISINOPRIL, HYDROCHLOROTHIAZIDE. Patient recovered.
Byetta Side Effects Report #5652320-0
Pharmacist from UNITED STATES reported BYETTA problem on Oct 17, 2007. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, weight increased, . BYETTA dosage: unknown. Patient recovered.
Enbrel Side Effects Report #5537286-6
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 09, 2006. Female patient, 20 years of age, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, urticaria, . ENBREL dosage: unknown. Patient recovered.
Enbrel Side Effects Report #5537295-7
Consumer or non-health professional from UNITED STATES reported ENBREL problem on Nov 07, 2006. Female patient, weighting 218.3 lb, was diagnosed with psoriatic arthropathy and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . ENBREL dosage: unknown. Patient recovered.
Enbrel Side Effects Report #5540409-6
ENBREL problem was reported by a Physician from UNITED STATES on July 10, 2007. Male patient, weighting 154.1 lb, was diagnosed with ankylosing spondylitis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, injection site swelling, . ENBREL dosage: unknown. During the same period patient was treated with PREDNISONE, CELEBREX. Patient recovered.
Enbrel Side Effects Report #5542076-4
Physician from UNITED STATES reported ENBREL problem on Dec 14, 2006. Female patient, weighting 160.9 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . ENBREL dosage: unknown. During the same period patient was treated with PLAQUENIL, NEURONTIN, AMITRIPTLINE, DARVOCET. Patient recovered.
Enbrel Side Effects Report #5542095-8
ENBREL problem was reported by a Physician from UNITED STATES on Feb 09, 2007. Female patient, weighting 126.1 lb, was diagnosed with psoriatic arthropathy and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . ENBREL dosage: unknown. Patient recovered.
Enbrel Side Effects Report #5548953-2
Consumer or non-health professional from UNITED STATES reported ENBREL problem on Mar 22, 2007. Female patient, weighting 121.0 lb, was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . ENBREL dosage: unknown. During the same period patient was treated with SELENIUM, METHOTREXATE, VITAMIN CAP. Patient recovered.
Humira Side Effects Report #5551465-3
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 03, 2007. Female patient, weighting 220.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, osteoarthritis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5559315-6
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Sept 20, 2007. Female patient, weighting 110.1 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 reaction, . HUMIRA dosage: unknown. During the same period patient was treated with AZATHIOPRINE, ENDOCORT AC. Patient recovered.
Humira Side Effects Report #5559462-9
HUMIRA problem was reported by a Health Professional from UNITED STATES on Oct 01, 2007. Female patient, weighting 118.1 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 reaction, . HUMIRA dosage: unknown. Patient recovered.
Humira Side Effects Report #5559602-1
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Nov 07, 2007. Female patient, weighting 140.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, rash, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, DURAGESIC, LORATADINE, FOLIC ACID, GABAPENTIN, SERTRALINE, ISONIAZID. Patient recovered.
Humira Side Effects Report #5559783-X
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2007. Female patient, weighting 110.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . HUMIRA dosage: unknown. Patient recovered.
Enbrel Side Effects Report #5562408-0
Physician from UNITED STATES reported ENBREL problem on Feb 08, 2007. Female patient, weighting 210.1 lb, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . ENBREL dosage: unknown. Patient recovered.
Kineret Side Effects Report #5562774-6
KINERET problem was reported by a Physician from AUSTRIA on Dec 04, 2007. Female patient, 32 years of age, was diagnosed with pre-existing disease and was treated with KINERET. After drug was administered, patient experienced the following problems/side effects: injection site reaction, interstitial lung disease, . KINERET dosage: unknown. During the same period patient was treated with COLCHICINE, MORPHINE. Patient was hospitalized. Patient recovered.
Boniva Side Effects Report #5514265-6
Pharmacist from UNITED STATES reported BONIVA problem on Sept 11, 2007. Female patient, 71 years of age, was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . BONIVA dosage: unknown. Patient was hospitalized. Patient recovered.
Levaquin Side Effects Report #5526321-7
LEVAQUIN problem was reported by a Pharmacist from UNITED STATES on Oct 20, 2006. Female patient was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . LEVAQUIN dosage: 500 MG, IN 1 DAY, INTRAVENOUS. Patient was hospitalized. Patient recovered.
Fuzeon Side Effects Report #5529304-6
Consumer or non-health professional from UNITED STATES reported FUZEON problem on Nov 19, 2007. Male patient, 46 years of age, weighting 160.1 lb, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: injection site reaction, lipodystrophy acquired, . FUZEON dosage: unknown. During the same period patient was treated with PREZISTA, TRUVADA, ZIAGEN, NORVIR. Patient recovered.
Augmentin Side Effects Report #5530328-3
AUGMENTIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 19, 2007. Female patient, 37 years of age, was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: injection site reaction, injection site urticaria, . AUGMENTIN dosage: unknown. Patient recovered.
Methotrexate Side Effects Report #5542549-4
Pharmacist from UNITED STATES reported METHOTREXATE problem on Apr 19, 2007. Male patient, child 5 years of age, was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . METHOTREXATE dosage: 12.5ML/SUBCUTANEOUSLY/ONCE A. Patient was hospitalized. Patient recovered.
Methotrexate Side Effects Report #5542556-1
METHOTREXATE problem was reported by a Consumer or non-health professional from UNITED STATES on May 24, 2007. Male patient, 16 years of age, was diagnosed with juvenile arthritis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . METHOTREXATE dosage: 1 ML SUBCUTANEOUSLY ONCE WEE OVER 1 YEAR (MOST RECENT DOSE 2. Patient recovered.
Methotrexate Side Effects Report #5542562-7
Health Professional from UNITED STATES reported METHOTREXATE problem on July 13, 2007. Female patient, 50 years of age, was diagnosed with rheumatoid arthritis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . METHOTREXATE dosage: 20MG/SUBCUTANEOUS/X ONCE WE. During the same period patient was treated with REMICADE, LEUCOVORIN, FOLIC ACID. Patient recovered.
Juvederm Side Effects Report #5477085-7
JUVEDERM problem was reported by a Health Professional from UNITED STATES on Oct 03, 2007. Female patient, 47 years of age, weighting 121.0 lb, was treated with JUVEDERM. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . JUVEDERM dosage: unknown. Patient recovered.
Rebif Side Effects Report #5477103-6
Pharmacist from UNITED STATES reported REBIF problem on Oct 03, 2007. Male patient was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . REBIF dosage: unknown. Patient recovered.
Betaseron Side Effects Report #5487090-2
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient, 39 years of age, weighting 150.0 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 reaction, multiple sclerosis, red blood cell count decreased, thyroid cancer, white blood cell count decreased, . BETASERON dosage: unknown. During the same period patient was treated with SYNTHROID, PREVACID, IBUPROFEN. Patient recovered.
Cyclophosphamide Side Effects Report #5487349-9
Consumer or non-health professional from reported CYCLOPHOSPHAMIDE problem on Oct 10, 2007. Female patient, 50 years of age, was diagnosed with breast cancer and was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: injection site reaction, necrosis, oedema peripheral, pain in extremity, paraesthesia, . CYCLOPHOSPHAMIDE dosage: unknown. During the same period patient was treated with FLUOROURACIL, EPIRUBICIN, CHLORIDE, HEPARIN OINTMENT. Patient was hospitalized. Patient recovered.
Leuprolide Side Effects Report #5490369-1
LEUPROLIDE ACETATE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 21, 2006. Female patient, 30 years of age, was diagnosed with infertility and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . LEUPROLIDE ACETATE dosage: unknown. Patient recovered.
Levemir Side Effects Report #5507365-8
Consumer or non-health professional from UNITED STATES reported LEVEMIR problem on Sept 14, 2007. Male patient was diagnosed with diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . LEVEMIR dosage: unknown. Patient recovered.
Levemir Side Effects Report #5508199-0
LEVEMIR problem was reported by a Health Professional from UNITED STATES on Aug 22, 2007. Female patient, 48 years of age, was diagnosed with insulin-requiring type ii diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . LEVEMIR dosage: unknown. During the same period patient was treated with NOVOLOG. Patient recovered.
Viraferonpeg Side Effects Report #5455179-X
Physician from FRANCE reported VIRAFERONPEG problem on Sept 05, 2007. Male patient, 54 years of age, weighting 189.6 lb, was diagnosed with hepatitis c and was treated with VIRAFERONPEG. After drug was administered, patient experienced the following problems/side effects: injection site reaction, panniculitis, skin necrosis, . VIRAFERONPEG dosage: unknown. During the same period patient was treated with REBETOL, AMARYL, GLUCOPHAGE, THERALENE. Patient recovered.
Betaseron Side Effects Report #5414382-5
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 02, 2007. Female patient, 39 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: injection site reaction, multiple sclerosis, red blood cell count decreased, thyroid cancer, white blood cell count decreased, . BETASERON dosage: unknown. During the same period patient was treated with SYNTHROID. Patient recovered.
Viraferonpeg Side Effects Report #5441502-9
Physician from FRANCE reported VIRAFERONPEG problem on Aug 17, 2007. Male patient, 43 years of age, was diagnosed with hepatitis c, neuropathy peripheral and was treated with VIRAFERONPEG. After drug was administered, patient experienced the following problems/side effects: injection site reaction, pruritus, rash maculo-papular, toxic skin eruption, . VIRAFERONPEG dosage: unknown. During the same period patient was treated with COPEGUS, LYRICA, REYATAZ, KALETRA, LAROXYL. Patient was hospitalized. Patient recovered.
Vaprisol Side Effects Report #5454246-4
VAPRISOL problem was reported by a Pharmacist from UNITED STATES on Mar 30, 2007. Female patient, 28 years of age, was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . VAPRISOL dosage: unknown. During the same period patient was treated with FENTANYL CITRATE. Patient recovered.
Fuzeon Side Effects Report #5390210-1
Consumer or non-health professional from UNITED STATES reported FUZEON problem on July 09, 2007. Male patient, 47 years of age, weighting 160.1 lb, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: injection site reaction, lipodystrophy acquired, . FUZEON dosage: unknown. During the same period patient was treated with PREZISTA, TRUVADA, ZIAGEN, NORVIR. Patient recovered.
Procrit Side Effects Report #5398479-4
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2007. Male patient, weighting 185.2 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: injection site reaction, joint swelling, oedema peripheral, . PROCRIT dosage: unknown. Patient recovered.
Levemir Side Effects Report #5423415-1
Physician from UNITED STATES reported LEVEMIR problem on May 03, 2007. Female patient was diagnosed with diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: injection site reaction, . LEVEMIR dosage: unknown. Patient recovered.