Menu

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

HYPERPLASIA side effect

What is HYPERPLASIA ?

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

Type your question here

 letters left

Tysabri Side Effects Report #5629021-8
Consumer or non-health professional from UNITED STATES reported TYSABRI problem on Jan 29, 2008. Female patient, 55 years of age, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: hyperplasia, impaired healing, injection site necrosis, open wound, skin necrosis, . TYSABRI dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX, BETASERON. Patient was hospitalized. Patient recovered.

Sorafenib Side Effects Report #5607863-2
SORAFENIB problem was reported by a Health Professional from UNITED STATES on Nov 02, 2007. Male patient, 39 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with SORAFENIB. After drug was administered, patient experienced the following problems/side effects: hyperplasia, . SORAFENIB dosage: TOTAL DAILY DOSE: 800 MG. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5567777-3
Health Professional from UNITED STATES reported NATALIZUMAB problem on Dec 10, 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: hyperplasia, impaired healing, injection site necrosis, open wound, skin disorder, skin hypertrophy, skin lesion, skin necrosis, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX, BETASERON. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5407167-7
FOSAMAX problem was reported by a Consumer or non-health professional from GERMANY on Aug 01, 2007. Female patient, 64 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hyperplasia, nasal disorder, nasal polyps, nasal septum deviation, osteitis, osteomyelitis, osteonecrosis, rhinitis, . FOSAMAX dosage: unknown. During the same period patient was treated with MAGNESIUM OROTATE, AMYLASE AND BROMELAINS AND CHYMOTRYPSIN AND LIPASE AND PANCREATIN AND, CALCIUM CITRATE AND CHOLECALCIFEROL, METOPROLOL SUCCINATE, PYRIDOXINE HYDROCHLORIDE AND THIAMINE HYDROCHLORIDE, ETILEFRINE, ATORVASTATIN CALCIUM. Patient was hospitalized and became disabled. Patient recovered.


Avonex Side Effects Report #5754169-7
Physician from SPAIN reported AVONEX problem on May 08, 2008. Male patient, 26 years of age, weighting 132.3 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hyperplasia, injury, petechiae, thrombocytopenic purpura, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Tamoxifen Side Effects Report #5265227-8
TAMOXIFEN CITRATE problem was reported by a Consumer or non-health professional from UNITED STATES on May 19, 2004. Female patient, 68 years of age, weighting 142.0 lb, was diagnosed with breast cancer and was treated with TAMOXIFEN CITRATE. After drug was administered, patient experienced the following problems/side effects: hyperplasia, ultrasound pelvis abnormal, . TAMOXIFEN CITRATE dosage: 20 MG PO. During the same period patient was treated with ATENOLOL, TRIAMTERENE, POTASSIUM CHLORIDE, ZOLOFT, COUMADIN, ATARAX, DIPHENHYDRAMINE. Patient recovered.

Plavix Side Effects Report #5621088-6
Consumer or non-health professional from UNITED STATES reported PLAVIX problem on Jan 09, 2007. Male patient was diagnosed with coronary artery disease, percutaneous coronary intervention and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: haematuria, hyperplasia, prostatitis, urethritis, . PLAVIX dosage: 75 MG QD - ORAL. During the same period patient was treated with ASPIRIN. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5513677-4
PROGRAF problem was reported by a Physician from JAPAN on Oct 26, 2007. Male patient, 23 years of age, was diagnosed with heart transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: coronary artery restenosis, hyperplasia, . PROGRAF dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL. Patient recovered.

Prograf Side Effects Report #5500643-8
Physician from UNITED STATES reported PROGRAF problem on Oct 10, 2007. Male patient, 48 years of age, was diagnosed with liver transplant, osteopenia and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: focal glomerulosclerosis, hyperplasia, kidney fibrosis, liver transplant rejection, osteopenia, renal tubular atrophy, renal vessel disorder, . PROGRAF dosage: ORAL; 9 MG, UID/QD, ORAL. During the same period patient was treated with CORTICOSTEROIDS, MYCOPHENOLATE MOFETIL, PREDNISONE, ALENDRONATE. Patient recovered.


Prempro Side Effects Report #5501576-3
PREMPRO problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2007. Female patient was treated with PREMPRO. After drug was administered, patient experienced the following problems/side effects: contralateral breast cancer, hyperplasia, . PREMPRO dosage: unknown. Patient recovered.

Stromectol Side Effects Report #5760350-3
Health Professional from FRANCE reported STROMECTOL problem on June 02, 2008. Male patient, 30 years of age, was treated with STROMECTOL. After drug was administered, patient experienced the following problems/side effects: dermatitis bullous, hyperplasia, rash pustular, urticaria, . STROMECTOL dosage: unknown. Patient was hospitalized. Patient recovered.

Diltiazem Side Effects Report #5740128-7
DILTIAZEM HYDROCHLORIDE problem was reported by a Health Professional from UNITED KINGDOM on Apr 28, 2008. Male patient, 63 years of age, was diagnosed with hypertension and was treated with DILTIAZEM HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: gingival bleeding, hyperplasia, . DILTIAZEM HYDROCHLORIDE dosage: (300 MG QD ORAL). During the same period patient was treated with OLMESARTAN MEDOXOMIL. Patient recovered.

Avonex Side Effects Report #5650407-X
Consumer or non-health professional from GERMANY reported AVONEX problem on Feb 18, 2008. Female patient, 56 years of age, weighting 202.8 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: depression, disease recurrence, hyperplasia, influenza like illness, ovarian cyst, restless legs syndrome, sleep apnoea syndrome, uterine cervix atrophy, uterine disorder, . AVONEX dosage: unknown. During the same period patient was treated with METAHEXAL, TRIAMTEREN, ALLOPURINOL, MYOCHOLINE, CITALOPRAM, MIRTAZAPINE, METFORMIN, CLIMOPAX. Patient was hospitalized. Patient recovered.

Prednisone Side Effects Report #5485890-6
PREDNISONE problem was reported by a Consumer or non-health professional from on Oct 09, 2007. Male patient, 64 years of age, was diagnosed with immunosuppression, alternaria infection and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: alternaria infection, haemorrhage, hyperplasia, scab, skin papilloma, . PREDNISONE dosage: unknown. During the same period patient was treated with TACROLIMUS, MYCOPHENOLATE MOFETIL, ITRACONAZOLE. Patient recovered.


Sutent Side Effects Report #5503231-2
Consumer or non-health professional from UNITED STATES reported SUTENT problem on Oct 23, 2007. Female patient, weighting 156.1 lb, was diagnosed with breast cancer metastatic and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: culture wound positive, gastroenteritis proteus, hyperplasia, infected skin ulcer, pseudomonas infection, skin graft, skin infection, skin odour abnormal, staphylococcal infection, . SUTENT dosage: unknown. During the same period patient was treated with PACLITAXEL, LOPERAMIDE, EPOETIN ALFA, NEUPOGEN, ULTRAM, ESOMEPRAZOLE MAGNESIUM, FEXOFENADINE, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5394893-1
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on July 13, 2007. Female patient, weighting 238.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: endometrial cancer, endometriosis, hyperplasia, . HUMIRA dosage: unknown. During the same period patient was treated with SULFASALAZINE, METHOTREXATE, DIHYDROCODEINE BITARTRATE, DICLOFENAC, FERROUS SULPHATE, FOLIC ACID, INSULIN LISPRO, HYDROXYCHLOROQUINE SULPHATE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5394893-1
Health Professional from UNITED KINGDOM reported HUMIRA problem on July 13, 2007. Female patient, weighting 238.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: endometrial cancer, endometriosis, hyperplasia, . HUMIRA dosage: unknown. During the same period patient was treated with SULFASALAZINE, METHOTREXATE, DIHYDROCODEINE BITARTRATE, DICLOFENAC, FERROUS SULPHATE, FOLIC ACID, INSULIN LISPRO, HYDROXYCHLOROQUINE SULPHATE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5271801-5
PROGRAF problem was reported by a Physician from JAPAN on Feb 28, 2007. Male patient, 48 years of age, was diagnosed with stem cell transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: aplasia pure red cell, bone marrow failure, hyperplasia, pancytopenia, trace element deficiency, . PROGRAF dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL. Patient recovered.

Prograf Side Effects Report #5282392-7
Physician from JAPAN reported PROGRAF problem on Mar 08, 2007. Male patient, 48 years of age, was diagnosed with stem cell transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: aplasia pure red cell, bone marrow failure, hyperplasia, pancytopenia, trace element deficiency, . PROGRAF dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL. Patient recovered.