Menu

• Ask a Health Expert about BREAST HAEMATOMA
• Post Your Side Effect related to BREAST HAEMATOMA
• BREAST HAEMATOMA and FDA Warnings
• BREAST HAEMATOMA in Patients Wiki
• Report BREAST HAEMATOMA in Drug Side Effect Survey

BREAST HAEMATOMA side effect

What is BREAST HAEMATOMA ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Arixtra Side Effects Report #5532085-3
Physician from FRANCE reported ARIXTRA problem on Nov 26, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: breast haematoma, fall, . ARIXTRA dosage: 7.5MG PER DAY. Patient recovered.

Augmentin Side Effects Report #5564949-9
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Dec 10, 2007. Female patient, 77 years of age, was diagnosed with infection, ventricular tachyarrhythmia and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: breast haematoma, international normalised ratio increased, . AUGMENTIN dosage: unknown. During the same period patient was treated with PREVISCAN, LASIX, LANTUS, DIFFU K, INEXIUM, FORLAX. Patient died.

Vidaza Side Effects Report #5766018-1
Physician from UNITED STATES reported VIDAZA problem on May 23, 2008. Female patient, 66 years of age, weighting 187.4 lb, was diagnosed with myelodysplastic syndrome and was treated with VIDAZA. After drug was administered, patient experienced the following problems/side effects: breast haematoma, ecchymosis, epistaxis, idiopathic thrombocytopenic purpura, injection site induration, injury, karyotype analysis abnormal, neutropenia, pancytopenia, . VIDAZA dosage: (50 MG/M2, DAILY X 10 DAYS), SUBCUTANEOUS. During the same period patient was treated with COMPAZINE, VITAMINS. Patient recovered.

Kaletra Side Effects Report #5794279-1
KALETRA problem was reported by a Consumer or non-health professional from BELGIUM on June 18, 2008. Female patient was diagnosed with hiv infection and was treated with KALETRA. After drug was administered, patient experienced the following problems/side effects: breast haematoma, fall, . KALETRA dosage: unknown. Patient was hospitalized. Patient recovered.


Warfarin Side Effects Report #5739776-X
Pharmacist from UNITED STATES reported WARFARIN problem on May 12, 2008. Female patient, 70 years of age, was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: breast haematoma, coagulopathy, epistaxis, international normalised ratio increased, . WARFARIN dosage: 5MG/10MG EVERY OTHER DAY PO. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5707076-X
LOVENOX problem was reported by a Pharmacist from UNITED STATES on Apr 14, 2008. Female patient, weighting 150.0 lb, was diagnosed with prophylaxis and was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: breast haematoma, . LOVENOX dosage: unknown. Patient recovered.

Aggrenox Side Effects Report #5625520-3
Physician from UNITED STATES reported AGGRENOX problem on Feb 11, 2008. Female patient, 80 years of age, was treated with AGGRENOX. After drug was administered, patient experienced the following problems/side effects: application site reaction, breast haematoma, . AGGRENOX dosage: unknown. During the same period patient was treated with NITROGLYCERIN. Patient recovered.

Forteo Side Effects Report #5744341-4
FORTEO problem was reported by a Physician from UNITED STATES on May 06, 2008. Female patient, weighting 150.0 lb, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: breast cancer, breast haematoma, . FORTEO dosage: unknown. During the same period patient was treated with VICODIN, NASAL SPRAY, GLUCOSAMINE, CALCIUM, ASPIRIN. Patient recovered.

Fosamax Side Effects Report #5622506-X
Physician from UNITED STATES reported FOSAMAX problem on Jan 31, 2008. Female patient, 54 years of age, weighting 167.6 lb, was diagnosed with osteoporosis prophylaxis, systemic lupus erythematosus and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: acute sinusitis, breast calcifications, breast haematoma, bursitis, cerumen impaction, costochondritis, cough, fall, fatigue, . FOSAMAX dosage: unknown. During the same period patient was treated with IMURAN, METHOTREXATE, FOLIC ACID, DARVOCET, VICODIN, CARDIZEM, AMITRIPTYLINE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.


Fosamax Side Effects Report #5776030-4
FOSAMAX problem was reported by a Physician from UNITED STATES on June 12, 2008. Female patient, 54 years of age, weighting 167.6 lb, was diagnosed with osteoporosis prophylaxis, systemic lupus erythematosus and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: acute sinusitis, breast calcifications, breast haematoma, bursitis, cerumen impaction, costochondritis, cough, deafness, fall, . FOSAMAX dosage: unknown. During the same period patient was treated with IMURAN, METHOTREXATE, FOLIC ACID, DARVOCET, VICODIN, CARDIZEM, AMITRIPTYLINE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5795623-1
Physician from UNITED STATES reported FOSAMAX problem on June 20, 2008. Female patient, 54 years of age, weighting 167.6 lb, was diagnosed with osteoporosis prophylaxis, systemic lupus erythematosus and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: acute sinusitis, breast calcifications, breast haematoma, bursitis, cerumen impaction, costochondritis, cough, deafness, fall, . FOSAMAX dosage: unknown. During the same period patient was treated with IMURAN, METHOTREXATE, FOLIC ACID, DARVOCET, VICODIN, CARDIZEM, AMITRIPTYLINE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5725210-2
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Apr 28, 2008. Female patient, 85 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, asthenia, breast haematoma, circulatory collapse, coagulopathy, hyperkalaemia, intra-abdominal haematoma, . ARIXTRA dosage: unknown. During the same period patient was treated with DEROXAT, DIFFU K, BURINEX, ALDACTONE, ATHYMIL. Patient was hospitalized. Patient died on 10/08/2007.