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INFUSION SITE REACTION side effect

What is INFUSION SITE REACTION ?
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Drugs associated with INFUSION SITE REACTION

ACETYLCYSTEINE  ALLOGENIC  AVELOX  AVONEX  CELEBREX  CLOZAPINE  ERBITUX  HEPARIN  IOPAMIDOL  LEVAQUIN  NATALIZUMAB  NEXIUM  ORENCIA  OXALIPLATIN  REBIF  REMICADE  RITUXAN  TAXOL  TRASYLOL  TYSABRI  VANCOMYCIN  VISUDYNE  VIVAGLOBIN  ZOFRAN  


Avelox Side Effects Report #5672358-7
Pharmacist from UNITED STATES reported AVELOX problem on Mar 18, 2008. Female patient was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, rash macular, . AVELOX dosage: 400MG ONCE IV. Patient recovered.

Avelox Side Effects Report #5640082-2
AVELOX problem was reported by a Pharmacist from UNITED STATES on Jan 27, 2008. Male patient, 84 years of age, weighting 143.3 lb, was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, injection site erythema, injection site irritation, injection site oedema, vessel puncture site pain, vessel puncture site reaction, . AVELOX dosage: unknown. Patient recovered.

Avonex Side Effects Report #5420427-9
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Aug 06, 2007. Male patient, 20 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Trasylol Side Effects Report #5461063-8
TRASYLOL problem was reported by a Physician from UNITED STATES on Nov 16, 2006. Female patient was treated with TRASYLOL. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . TRASYLOL dosage: unknown. Patient recovered.


Vancomycin Side Effects Report #5381480-4
Health Professional from UNITED STATES reported VANCOMYCIN problem on July 05, 2007. Female patient, weighting 136.7 lb, was diagnosed with cellulitis and was treated with VANCOMYCIN. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, injection site reaction, . VANCOMYCIN dosage: 826MG. Patient recovered.

Vancomycin Side Effects Report #5381480-4
VANCOMYCIN problem was reported by a Health Professional from UNITED STATES on July 05, 2007. Female patient, weighting 136.7 lb, was diagnosed with cellulitis and was treated with VANCOMYCIN. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, injection site reaction, . VANCOMYCIN dosage: 826MG. Patient recovered.

Orencia Side Effects Report #5795146-X
Consumer or non-health professional from UNITED STATES reported ORENCIA problem on May 13, 2008. Female patient was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . ORENCIA dosage: unknown. Patient recovered.

Zofran Side Effects Report #5309724-5
ZOFRAN problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2006. Female patient, 25 years of age, was treated with ZOFRAN. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . ZOFRAN dosage: 4MG PER DAY. During the same period patient was treated with PITOCIN, NARCAN, LACTATED RINGER. Patient recovered.

Taxol Side Effects Report #5252307-6
Consumer or non-health professional from UNITED STATES reported TAXOL problem on Mar 10, 2006. Female patient, 48 years of age, weighting 379.2 lb, was diagnosed with lung neoplasm malignant and was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . TAXOL dosage: unknown. During the same period patient was treated with DECADRON, KYTRIL. Patient was hospitalized. Patient recovered.


Erbitux Side Effects Report #5252464-1
ERBITUX problem was reported by a Health Professional from UNITED STATES on Nov 17, 2006. Male patient, 82 years of age, weighting 134.5 lb, was diagnosed with nasal cavity cancer and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . ERBITUX dosage: unknown. During the same period patient was treated with BENADRYL. Patient recovered.

Erbitux Side Effects Report #5252496-3
Consumer or non-health professional from UNITED STATES reported ERBITUX problem on Dec 21, 2006. Female patient, 52 years of age, weighting 116.8 lb, was diagnosed with laryngeal cancer and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . ERBITUX dosage: unknown. During the same period patient was treated with CARBOPLATIN, TAXOTERE, FLUOROURACIL. Patient recovered.

Nexium Side Effects Report #5265155-8
NEXIUM IV problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 13, 2006. Male patient, 61 years of age, was treated with NEXIUM IV. After drug was administered, patient experienced the following problems/side effects: infusion site reaction, . NEXIUM IV dosage: unknown. Patient recovered.

Avelox Side Effects Report #5629485-X
Pharmacist from UNITED STATES reported AVELOX problem on Feb 13, 2008. Male patient, 77 years of age, was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: infusion site discolouration, infusion site reaction, . AVELOX dosage: unknown. Patient recovered.

Allogenic Side Effects Report #5483572-8
ALLOGENIC PERIPHERAL BLOOD STEM CELL DONOR problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 09, 2007. Male patient, weighting 313.1 lb, was treated with ALLOGENIC PERIPHERAL BLOOD STEM CELL DONOR. After drug was administered, patient experienced the following problems/side effects: coma, infusion site reaction, subdural haematoma, . ALLOGENIC PERIPHERAL BLOOD STEM CELL DONOR dosage: unknown. During the same period patient was treated with NEUPOGEN, ACID CITRATE DEXTROSE SOLUTION, HEPARIN. Patient was hospitalized. Patient died.


Levaquin Side Effects Report #5504773-6
Health Professional from UNITED STATES reported LEVAQUIN problem on Oct 31, 2007. Female patient was diagnosed with abdominal pain, cystitis, hypovolaemia, multiple sclerosis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: infusion site erythema, infusion site reaction, pain in extremity, . LEVAQUIN dosage: 500MG (IV) DAILY. Patient recovered.

Oxaliplatin Side Effects Report #5465440-0
OXALIPLATIN problem was reported by a Health Professional from UNITED STATES on Sept 20, 2007. Male patient, 26 years of age, weighting 129.0 lb, was diagnosed with gastric cancer and was treated with OXALIPLATIN. After drug was administered, patient experienced the following problems/side effects: feeding tube complication, infusion site reaction, nausea, vomiting, . OXALIPLATIN dosage: unknown. During the same period patient was treated with LEUCOVORIN, FLUOROURACIL. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5389278-8
Health Professional from CANADA reported REMICADE problem on July 06, 2007. Female patient, 70 years of age, was diagnosed with psoriatic arthropathy and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: eye operation, infusion site reaction, . REMICADE dosage: unknown. Patient recovered.

Remicade Side Effects Report #5389278-8
REMICADE problem was reported by a Health Professional from CANADA on July 06, 2007. Female patient, 70 years of age, was diagnosed with psoriatic arthropathy and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: eye operation, infusion site reaction, . REMICADE dosage: unknown. Patient recovered.

Heparin Side Effects Report #5787385-9
Health Professional from UNITED STATES reported HEPARIN problem on June 25, 2008. Male patient, 64 years of age, weighting 346.0 lb, was diagnosed with evidence based treatment and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: epistaxis, infusion site reaction, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.


Levaquin Side Effects Report #5737042-X
LEVAQUIN problem was reported by a Pharmacist from UNITED STATES on May 12, 2008. Female patient, 50 years of age, was diagnosed with pneumonia and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: feeling hot, infusion site reaction, rash pruritic, . LEVAQUIN dosage: 750MG IV. Patient recovered.

Levaquin Side Effects Report #5737043-1
Pharmacist from UNITED STATES reported LEVAQUIN problem on May 12, 2008. Female patient, 43 years of age, was diagnosed with pneumonia and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: feeling hot, infusion site reaction, pain in extremity, rash, . LEVAQUIN dosage: 750MG IV. Patient recovered.

Acetylcysteine Side Effects Report #5368810-4
ACETYLCYSTEINE problem was reported by a Pharmacist from UNITED STATES on June 22, 2007. Male patient, 47 years of age, weighting 171.1 lb, was diagnosed with overdose and was treated with ACETYLCYSTEINE. After drug was administered, patient experienced the following problems/side effects: infusion site erythema, infusion site reaction, infusion site swelling, . ACETYLCYSTEINE dosage: ACETYLCYSTEINE 3880MG/500ML OVER 4 HR X 1 IV DRIP. Patient recovered.

Rituxan Side Effects Report #5266769-1
Consumer or non-health professional from UNITED STATES reported RITUXAN problem on Mar 01, 2007. Male patient, 87 years of age, was diagnosed with lymphoma and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, infusion site reaction, loss of consciousness, pulse absent, transient ischaemic attack, urinary incontinence, white blood cell count increased, . RITUXAN dosage: 600 MG, 1/WEEK, INTRAVENOUS. During the same period patient was treated with DECADRON, TYLENOL, BENADRYL. Patient recovered.

Tysabri Side Effects Report #5644375-4
TYSABRI problem was reported by a Health Professional from UNITED STATES on Feb 13, 2008. Male patient, 44 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: fall, hip fracture, infusion site reaction, postoperative wound infection, staphylococcal infection, urticaria, . TYSABRI dosage: 300 MG; QM; IV. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5530023-0
Consumer or non-health professional from UNITED STATES reported NATALIZUMAB problem on Nov 15, 2007. Female patient, 55 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: chest discomfort, dysphagia, infusion site reaction, tongue disorder, urticaria, . NATALIZUMAB dosage: unknown. Patient recovered.

Clozapine Side Effects Report #5531370-9
CLOZAPINE problem was reported by a Health Professional from ITALY on Nov 13, 2007. Male patient, 36 years of age, was diagnosed with mental disorder and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: electrolyte imbalance, febrile neutropenia, infusion site reaction, leukopenia, nephropathy toxic, pruritus, rash maculo-papular, skin exfoliation, . CLOZAPINE dosage: unknown. During the same period patient was treated with FLUCONAZOLE, LITHIUM CARBONATE, CITALOPRAM HYDROBROMIDE, CLOMIPRAMINE, LORAZEPAM. Patient was hospitalized. Patient recovered.

Iopamidol Side Effects Report #5398998-0
Pharmacist from UNITED STATES reported IOPAMIDOL problem on July 02, 2007. Female patient, 48 years of age, weighting 207.2 lb, was diagnosed with computerised tomogram and was treated with IOPAMIDOL. After drug was administered, patient experienced the following problems/side effects: blister, infusion site cellulitis, infusion site reaction, paraesthesia, tendon pain, . IOPAMIDOL dosage: 150 MG IV X 1. Patient was hospitalized. Patient recovered.

Iopamidol Side Effects Report #5398998-0
IOPAMIDOL problem was reported by a Pharmacist from UNITED STATES on July 02, 2007. Female patient, 48 years of age, weighting 207.2 lb, was diagnosed with computerised tomogram and was treated with IOPAMIDOL. After drug was administered, patient experienced the following problems/side effects: blister, infusion site cellulitis, infusion site reaction, paraesthesia, tendon pain, . IOPAMIDOL dosage: 150 MG IV X 1. Patient was hospitalized. Patient recovered.

Celebrex Side Effects Report #5792608-6
Consumer or non-health professional from UNITED STATES reported CELEBREX problem on June 16, 2008. Female patient, weighting 145.1 lb, was diagnosed with arthritis, blood cholesterol and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, dissociation, infusion site reaction, pulmonary embolism, . CELEBREX dosage: unknown. During the same period patient was treated with CENTRUM SILVER, MAXZIDE, OMEGA, NITROTAB, GLUCOSAMINE W, LIPITOR, FISH OIL. Patient was hospitalized. Patient recovered.

Vivaglobin Side Effects Report #5325023-X
VIVAGLOBIN problem was reported by a Pharmacist from UNITED STATES on May 11, 2007. Female patient, weighting 165.3 lb, was diagnosed with congenital hypogammaglobulinaemia and was treated with VIVAGLOBIN. After drug was administered, patient experienced the following problems/side effects: infusion site erythema, infusion site reaction, infusion site swelling, skin irritation, . VIVAGLOBIN dosage: 7.36 GRAMS -46 ML- EVERY 7 DAYS SQ. Patient recovered.

Rebif Side Effects Report #5347706-8
Health Professional from UNITED STATES reported REBIF problem on Sept 01, 2006. Male patient, 23 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: asthenia, diplopia, infusion site reaction, infusion site warmth, multiple sclerosis, oedema peripheral, pain in extremity, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Visudyne Side Effects Report #5139980-8
VISUDYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 12, 2006. Male patient, 80 years of age, weighting 137.0 lb, was treated with VISUDYNE. After drug was administered, patient experienced the following problems/side effects: infusion site discolouration, infusion site pain, infusion site reaction, syncope vasovagal, . VISUDYNE dosage: unknown. During the same period patient was treated with PLAVIX, PREVACID, FLOMAX, ASPIRIN, FOLIC ACID, NITROGLYCERIN, ZESTRIL, NORVASC. Patient was hospitalized. Patient recovered.

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