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INJECTION SITE HAEMATOMA side effect

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Lucrin Side Effects Report #5618235-9
Consumer or non-health professional from AUSTRALIA reported LUCRIN DEPOT problem on Jan 28, 2008. Male patient, 84 years of age, was diagnosed with prostate cancer and was treated with LUCRIN DEPOT. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, injection site mass, injection site necrosis, . LUCRIN DEPOT dosage: 22.5 MG (22.5 MG (LEUPROLIDE ACETATE). During the same period patient was treated with ASPIRIN, NICORANDIL, DIGOXIN, SOTALOL HYDROCHLORIDE, SIMVASTATIN. Patient recovered.

Lupron Side Effects Report #5634228-X
LUPRON DEPOT problem was reported by a Pharmacist from UNITED STATES on Feb 20, 2008. Male patient, 63 years of age, weighting 191.0 lb, was diagnosed with prostate cancer and was treated with LUPRON DEPOT. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, . LUPRON DEPOT dosage: unknown. During the same period patient was treated with LUPRON DEPOT, LUPRON DEPOT. Patient recovered.

Lovenox Side Effects Report #5593099-0
Consumer or non-health professional from FRANCE reported LOVENOX problem on Jan 07, 2008. Female patient, 68 years of age, was diagnosed with thrombosis prophylaxis and was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, retinal vein occlusion, thrombosis, . LOVENOX dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Byetta Side Effects Report #5533787-5
BYETTA problem was reported by a Consumer or non-health professional from COLOMBIA on Nov 27, 2007. Female patient, 67 years of age, was diagnosed with diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, pneumonia, . BYETTA dosage: unknown. During the same period patient was treated with GLIMEPIRIDE, LANTUS, SERETIDE, IPRATROPIUM BROMIDE. Patient was hospitalized. Patient recovered.


Byetta Side Effects Report #5502234-1
Consumer or non-health professional from COLOMBIA reported BYETTA problem on Oct 19, 2007. Female patient, 67 years of age, was diagnosed with diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, pneumonia, . BYETTA dosage: unknown. During the same period patient was treated with GLIMEPIRIDE, LANTUS, SERETIDE, IPRATROPIUM BROMIDE. Patient was hospitalized. Patient recovered.

Novorapid Side Effects Report #5715830-3
NOVORAPID problem was reported by a Health Professional from FRANCE on Apr 14, 2008. Male patient, child 11 years of age, was diagnosed with type 1 diabetes mellitus and was treated with NOVORAPID. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, injection site reaction, injection site urticaria, . NOVORAPID dosage: unknown. During the same period patient was treated with LEVEMIR. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5719483-X
Consumer or non-health professional from FRANCE reported LOVENOX problem on Apr 24, 2008. Female patient, 68 years of age, was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, retinal vein occlusion, . LOVENOX dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Lovenox Side Effects Report #5368848-7
LOVENOX problem was reported by a Pharmacist from UNITED STATES on June 21, 2007. Female patient, weighting 198.4 lb, was diagnosed with atrial fibrillation and was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, muscle haemorrhage, . LOVENOX dosage: 90MG Q12H SQ. Patient was hospitalized. Patient recovered.

Zoladex Side Effects Report #5316731-5
Physician from JAPAN reported ZOLADEX problem on May 01, 2007. Male patient was diagnosed with prostate cancer and was treated with ZOLADEX. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, . ZOLADEX dosage: unknown. During the same period patient was treated with LEUPROLIDE ACETATE. Patient recovered.


Heparin Side Effects Report #5351615-8
HEPARIN problem was reported by a Health Professional from UNITED STATES on Mar 22, 2007. Female patient, 36 years of age, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5283391-1
Consumer or non-health professional from FRANCE reported LOVENOX problem on Mar 23, 2007. Female patient, 68 years of age, was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, retinal vascular thrombosis, . LOVENOX dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Rocephin Side Effects Report #5296367-5
ROCEPHIN problem was reported by a Pharmacist from FRANCE on Apr 02, 2007. Female patient, 86 years of age, was diagnosed with lung infection, atrial fibrillation and was treated with ROCEPHIN. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, injection site rash, oedema peripheral, pain in extremity, . ROCEPHIN dosage: unknown. During the same period patient was treated with CARDENSIEL, AMIODARONE, ANTICOAGULANT, LASIX, DIFFU, SOLUPRED, FURADANTIN, COUMADIN. Patient was hospitalized. Patient recovered.

Levemir Side Effects Report #5346263-X
Consumer or non-health professional from UNITED STATES reported LEVEMIR problem on Jan 03, 2007. Male patient, 83 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 haematoma, . LEVEMIR dosage: unknown. During the same period patient was treated with METFORMIN, STARLIX. Patient recovered.

Arixtra Side Effects Report #5615122-7
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site haematoma, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.


Avonex Side Effects Report #5599221-4
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Jan 08, 2008. Female patient, 44 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: influenza like illness, injection site haematoma, injection site reaction, thrombosis, tremor, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5604098-4
LOVENOX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2008. Female patient, weighting 152.1 lb, was diagnosed with hypertension and was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: haematoma, injection site haematoma, oedema peripheral, pain in extremity, skin discolouration, . LOVENOX dosage: unknown. During the same period patient was treated with COZAAR, TIAZAC, DIAZIDE, GLIPIZIDE, ACTONEL, PREVACID. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5545635-8
Consumer or non-health professional from UNITED STATES reported LOVENOX problem on Dec 05, 2007. Female patient was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: haematoma, injection site haematoma, oedema peripheral, pain in extremity, skin discolouration, . LOVENOX dosage: unknown. During the same period patient was treated with COZAAR, TIAZAC, DIAZIDE, GLIPIZIDE, ACTONEL, PREVACID. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5558726-2
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 04, 2007. Female patient 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 haematoma, . HUMIRA dosage: unknown. Patient recovered.

Copaxone Side Effects Report #5522857-3
Consumer or non-health professional from GERMANY reported COPAXONE problem on Nov 01, 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: abdominal wall infection, injection site haematoma, injection site inflammation, injection site necrosis, injection site pain, muscle twitching, . COPAXONE dosage: 20 MG (20 MG, 1 IN 1 D), SUBCUTANEOUS. During the same period patient was treated with PHENPROCOUMON. Patient was hospitalized. Patient recovered.


Copaxone Side Effects Report #5484397-X
COPAXONE problem was reported by a Health Professional from GERMANY on Sept 24, 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: abdominal wall infection, injection site haematoma, injection site necrosis, muscle twitching, . COPAXONE dosage: 20 MG (20 MG, 1 IN 1 D) SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5486784-2
Physician from JAPAN reported ARIXTRA problem on Oct 15, 2007. Female patient, 80 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: ileus, injection site haematoma, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.

Arixtra Side Effects Report #5406073-1
ARIXTRA problem was reported by a Health Professional from GERMANY on Aug 02, 2007. Female patient, 45 years of age, weighting 169.8 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain lower, injection site haematoma, injection site pain, . ARIXTRA dosage: .75MG PER DAY. During the same period patient was treated with MARCUMAR. Patient recovered.

Boniva Side Effects Report #5452360-0
Physician from UNITED STATES reported BONIVA problem on Apr 19, 2007. Female patient, 79 years of age, weighting 121.9 lb, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: injection site erythema, injection site haematoma, injection site mass, injection site pain, injection site swelling, . BONIVA dosage: 3 MG INTRAVENOUS BOLUS. Patient recovered.

Byetta Side Effects Report #5426553-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 21, 2007. Female patient, 59 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 erythema, injection site haematoma, injection site nodule, injection site pain, injection site pruritus, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ACTOS. Patient recovered.

Byetta Side Effects Report #5426553-2
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Apr 21, 2007. Female patient, 59 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 erythema, injection site haematoma, injection site nodule, injection site pain, injection site pruritus, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ACTOS. Patient recovered.

Byetta Side Effects Report #5774333-0
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 28, 2008. Female patient, 65 years of age, was diagnosed with insulin resistance and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: epistaxis, injection site haematoma, . BYETTA dosage: unknown. Patient recovered.

Voltaren Side Effects Report #5269553-8
Physician from FRANCE reported VOLTAREN problem on Mar 13, 2007. Male patient, 90 years of age, weighting 154.3 lb, was diagnosed with sciatica and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: haematoma, injection site haematoma, injection site pain, muscle haemorrhage, . VOLTAREN dosage: 75 MG, UNK. During the same period patient was treated with ACETAMINOPHEN, STRESAM, TANAKAN, PERMIXON, PHYSIOTENS, RANITIDINE, CLARITIN. Patient was hospitalized. Patient recovered.

Heparin Side Effects Report #5625739-1
HEPARIN problem was reported by a Pharmacist from UNITED STATES on Feb 14, 2008. Female patient, weighting 170.0 lb, was diagnosed with thrombosis prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: blister, injection site bruising, injection site haematoma, rash erythematous, skin lesion, . HEPARIN dosage: HEPARIN (1ML 5000) Q8HR SQ (9 DOSES). Patient was hospitalized. Patient recovered.

Copaxone Side Effects Report #5476679-2
Consumer or non-health professional from GERMANY reported COPAXONE problem on Sept 24, 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: abdominal wall infection, cellulitis, injection site haematoma, injection site inflammation, injection site necrosis, injection site pain, muscle twitching, . COPAXONE dosage: 20 MG (20 MG, 1 IN 1 D). Patient was hospitalized. Patient recovered.

Xolair Side Effects Report #5426013-9
XOLAIR problem was reported by a Physician from SWITZERLAND on Aug 13, 2007. Female patient was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: asthma, dyspnoea, injection site haematoma, pharyngeal oedema, pruritus, . XOLAIR dosage: 300 MG, 2/MONTH. During the same period patient was treated with STEROIDS, BRONCHODILATORS. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5385346-5
Consumer or non-health professional from UNITED STATES reported LOVENOX problem on July 09, 2007. Female patient, 56 years of age, weighting 205.0 lb, was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: impaired healing, incision site complication, injection site haematoma, . LOVENOX dosage: 1 ML. TWICE PER DAY SQ. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5385346-5
LOVENOX problem was reported by a Consumer or non-health professional from UNITED STATES on July 09, 2007. Female patient, 56 years of age, weighting 205.0 lb, was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: impaired healing, incision site complication, injection site haematoma, . LOVENOX dosage: 1 ML. TWICE PER DAY SQ. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5744245-7
Consumer or non-health professional from UNITED STATES reported LOVENOX problem on May 13, 2008. Female patient, weighting 194.0 lb, was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: haematocrit decreased, haematoma, injection site haematoma, injection site haemorrhage, international normalised ratio increased, . LOVENOX dosage: unknown. During the same period patient was treated with COUMADIN. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5365677-5
ENBREL problem was reported by a Physician from UNITED STATES on June 13, 2007. Female patient, weighting 206.1 lb, was diagnosed with rheumatoid arthritis, psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: hypothyroidism, injection site haematoma, injection site haemorrhage, injection site pain, psoriasis, . ENBREL dosage: unknown. During the same period patient was treated with SYNTHROID, VITAMIN D, AMITRIPTYLINE. Patient recovered.

Byetta Side Effects Report #5364241-1
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Jan 09, 2007. Female patient, 59 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: feeling hot, injection site bruising, injection site haematoma, injection site nodule, nausea, oedema peripheral, rash pruritic, vomiting, . BYETTA dosage: unknown. Patient recovered.

Rebif Side Effects Report #5301506-3
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 05, 2007. Female patient, 46 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: catheter site haemorrhage, deep vein thrombosis, injection site haematoma, international normalised ratio increased, multiple sclerosis, post procedural haemorrhage, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5301508-7
Consumer or non-health professional from UNITED STATES reported REBIF problem on Apr 05, 2007. Female patient, 46 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: catheter related complication, deep vein thrombosis, injection site haematoma, international normalised ratio increased, multiple sclerosis, post procedural haemorrhage, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Angiomax Side Effects Report #5278771-4
ANGIOMAX problem was reported by a Physician from UNITED STATES on Mar 09, 2007. Female patient, 92 years of age, was diagnosed with percutaneous coronary intervention and was treated with ANGIOMAX. After drug was administered, patient experienced the following problems/side effects: femoral artery occlusion, iatrogenic injury, injection site haematoma, respiratory failure, . ANGIOMAX dosage: unknown. Patient died.