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EXCESSIVE GRANULATION TISSUE side effect

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Bortezomib Side Effects Report #5542046-6
Physician from TURKEY reported BORTEZOMIB problem on Dec 04, 2007. Female patient, 45 years of age, weighting 178.6 lb, was treated with BORTEZOMIB. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, osteonecrosis, tooth extraction, . BORTEZOMIB dosage: unknown. During the same period patient was treated with ZOMETA. Patient recovered.

Iressa Side Effects Report #5529580-X
IRESSA problem was reported by a Physician from JAPAN on Nov 22, 2007. Female patient, 60 years of age, was diagnosed with lung adenocarcinoma and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, rash, stomatitis, . IRESSA dosage: unknown. Patient recovered.

Gleevec Side Effects Report #5434305-2
Physician from GERMANY reported GLEEVEC problem on Aug 28, 2007. Female patient, 60 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, skin atrophy, skin erosion, skin ulcer, . GLEEVEC dosage: 400 MG, QD. Patient recovered.

Claravis Side Effects Report #5442538-4
CLARAVIS problem was reported by a Physician from UNITED STATES on Aug 16, 2007. Male patient, 16 years of age, was diagnosed with acne cystic and was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, pain of skin, . CLARAVIS dosage: 60 MG, QD, ORAL; 60 MG, BID, ORAL. Patient recovered.


Orlistat Side Effects Report #5760998-6
Consumer or non-health professional from UNITED KINGDOM reported ORLISTAT problem on June 03, 2008. Male patient, weighting 220.5 lb, was diagnosed with obesity, fluid retention and was treated with ORLISTAT. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, . ORLISTAT dosage: unknown. During the same period patient was treated with PERINDOPRIL, ATORVASTATIN, FUROSEMIDE, FELODIPINE, MIXTARD. Patient was hospitalized. Patient recovered.

Iressa Side Effects Report #5739500-0
IRESSA problem was reported by a Pharmacist from JAPAN on May 09, 2008. Male patient, 66 years of age, was diagnosed with lung neoplasm malignant and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, rash, . IRESSA dosage: unknown. Patient recovered.

Lioresal Side Effects Report #5757797-8
Physician from JAPAN reported LIORESAL problem on May 09, 2008. Male patient, weighting 58.20 lb, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, fistula, tracheal haemorrhage, tracheal obstruction, . LIORESAL dosage: unknown. During the same period patient was treated with FAMOTIDINE, PHENOBARBITAL, GALANTASE, ENTERONON, AZULENE, GASMOTIN, GLYSENNID. Patient died.

Adalat Side Effects Report #5347320-4
ADALAT problem was reported by a Health Professional from JAPAN on May 28, 2007. Male patient, 71 years of age, was diagnosed with aplastic anaemia and was treated with ADALAT. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, . ADALAT dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient was hospitalized. Patient recovered.

Skin Side Effects Report #5369003-7
Physician from UNITED STATES reported SKIN problem on Apr 24, 2007. Female patient, 58 years of age, was treated with SKIN. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, graft complication, inflammation, wound drainage, . SKIN dosage: unknown. Patient recovered.


Humira Side Effects Report #5332725-8
HUMIRA problem was reported by a Physician from FRANCE on May 14, 2007. Female patient, weighting 138.9 lb, was diagnosed with rheumatoid arthritis, hypercholesterolaemia, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, granuloma skin, injection site pruritus, injection site rash, oedema, purpura, vasculitis, . HUMIRA dosage: unknown. During the same period patient was treated with FLUVASTATIN, EPROSARTAN, PREDNISONE, METHOTREXATE, ACETAMINOPHEN W. Patient recovered.

Skin Side Effects Report #5335532-5
Physician from UNITED STATES reported SKIN problem on Apr 24, 2007. Female patient, 58 years of age, was treated with SKIN. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, inflammation, secretion discharge, . SKIN dosage: unknown. Patient recovered.

Cilostazol Side Effects Report #5291445-9
CILOSTAZOL problem was reported by a Consumer or non-health professional from JAPAN on Mar 19, 2007. Male patient, 59 years of age, was diagnosed with cerebral infarction and was treated with CILOSTAZOL. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, gastrointestinal erosion, melaena, . CILOSTAZOL dosage: 200 MG ORAL. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5254891-5
Physician from GERMANY reported ZOMETA problem on Feb 20, 2007. Female patient, 67 years of age, was diagnosed with metastases to bone, breast cancer metastatic, anxiety disorder and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, lip and/or oral cavity cancer, malignant tumour excision, osteonecrosis, sequestrectomy, suture insertion, tooth extraction, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with ARIMIDEX, NEXIUM, KALINOR, TORSEMIDE, DOXEPIN, LORAZEPAM, DURAGESIC. Patient recovered.

Aredia Side Effects Report #5263359-1
AREDIA problem was reported by a Physician from NETHERLANDS on Mar 01, 2007. Female patient, 83 years of age, was diagnosed with hypercalcaemia and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, osteitis, osteonecrosis, sequestrectomy, . AREDIA dosage: 15 MG/ML, QMO. During the same period patient was treated with TEMAZEPAM, METOPROLOL SUCCINATE, PERINDOPRIL ERBUMINE, FUROSEMIDE. Patient recovered.


Zometa Side Effects Report #5589253-4
Consumer or non-health professional from FRANCE reported ZOMETA problem on Jan 04, 2008. Female patient, 62 years of age, was diagnosed with complex regional pain syndrome and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone disorder, excessive granulation tissue, osteonecrosis, tooth resorption, x-ray abnormal, . ZOMETA dosage: 4 MG. During the same period patient was treated with LYRICA, NEURONTIN, RIVOTRIL, BROMAZEPAM, VITAMIN B. Patient recovered.

Zometa Side Effects Report #5562720-5
ZOMETA problem was reported by a Consumer or non-health professional from JAPAN on Dec 12, 2007. Female patient, 74 years of age, was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, excessive granulation tissue, excoriation, gingival erosion, impaired healing, osteonecrosis, primary sequestrum, tooth extraction, wound debridement, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA, MEDROXYPROGESTERONE ACETATE. Patient died on 10/30/2006.

Zometa Side Effects Report #5513788-3
Consumer or non-health professional from JAPAN reported ZOMETA problem on Nov 09, 2007. Female patient, 74 years of age, was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, excessive granulation tissue, excoriation, gingival erosion, impaired healing, osteonecrosis, primary sequestrum, tooth extraction, wound debridement, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA, MEDROXYPROGESTERONE ACETATE. Patient died on 10/30/2006.

Gleevec Side Effects Report #5497361-1
GLEEVEC problem was reported by a Physician from GERMANY on Oct 17, 2007. Female patient, weighting 297.6 lb, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: dermatitis, excessive granulation tissue, skin atrophy, skin erosion, skin ulcer, . GLEEVEC dosage: 400 MG, QD. Patient recovered.

Zoledronic Side Effects Report #5456127-9
Physician from UNITED KINGDOM reported ZOLEDRONIC ACID problem on Sept 13, 2007. Female patient, weighting 181.0 lb, was diagnosed with metastases to bone and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bacterial infection, excessive granulation tissue, mucosal inflammation, osteomyelitis chronic, osteonecrosis, pain in jaw, . ZOLEDRONIC ACID dosage: 4 MG. During the same period patient was treated with CALCIUM, VITAMIN D, WARFARIN, EPIRUBICIN, CYCLOPHOSPHAMIDE, DEXAMETHASONE. Patient recovered.


Zoledronic Side Effects Report #5410807-X
ZOLEDRONIC ACID problem was reported by a Physician from UNITED KINGDOM on July 30, 2007. Female patient, weighting 181.0 lb, was diagnosed with metastases to bone and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bacterial infection, excessive granulation tissue, mucosal inflammation, osteomyelitis chronic, osteonecrosis, pain in jaw, . ZOLEDRONIC ACID dosage: 4 MG. During the same period patient was treated with CALCIUM CHLORIDE, VITAMIN D, WARFARIN, EPIRUBICIN, CYCLOPHOSPHAMIDE, DEXAMETHASONE. Patient recovered.

Zometa Side Effects Report #5414862-2
Consumer or non-health professional from GERMANY reported ZOMETA problem on Aug 10, 2007. Male patient, 72 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: antibiotic prophylaxis, excessive granulation tissue, histology abnormal, oral surgery, osteonecrosis, pain, purulence, tooth extraction, wound dehiscence, . ZOMETA dosage: 4 MG, QD. During the same period patient was treated with CLINDAMYCIN, CEFUROXIME, MORPHINE SULPHATE, BISOHEXAL, ASPIRIN, PANTOPRAZOLE, CELEBREX, DYNACIL. Patient recovered.

Zoledronic Side Effects Report #5419646-7
ZOLEDRONIC ACID problem was reported by a Physician from UNITED KINGDOM on Aug 10, 2007. Female patient, weighting 181.0 lb, was diagnosed with metastases to bone and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bacterial infection, excessive granulation tissue, mucosal inflammation, osteomyelitis chronic, osteonecrosis, pain in jaw, . ZOLEDRONIC ACID dosage: 4 MG. During the same period patient was treated with CALCIUM CHLORIDE, VITAMIN D, WARFARIN, EPIRUBICIN, CYCLOPHOSPHAMIDE, DEXAMETHASONE. Patient recovered.

Zometa Side Effects Report #5693207-7
Consumer or non-health professional from FRANCE reported ZOMETA problem on Mar 25, 2008. Female patient, 62 years of age, was diagnosed with complex regional pain syndrome and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone disorder, excessive granulation tissue, osteomyelitis, osteonecrosis, tooth resorption, x-ray abnormal, . ZOMETA dosage: 4 MG. During the same period patient was treated with LYRICA, NEURONTIN, RIVOTRIL, BROMAZEPAM, VITAMIN B. Patient recovered.

Fosamax Side Effects Report #5706387-1
FOSAMAX problem was reported by a Physician from UNITED STATES on Apr 09, 2008. Female patient, 63 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: ear pain, excessive granulation tissue, inflammation, joint injury, lung disorder, osteomyelitis, osteonecrosis, pyrexia, road traffic accident, . FOSAMAX dosage: unknown. During the same period patient was treated with ALBUTEROL. Patient was hospitalized and became disabled. Patient recovered.

Zometa Side Effects Report #5503648-6
Consumer or non-health professional from JAPAN reported ZOMETA problem on Oct 24, 2007. Female patient, 54 years of age, weighting 105.8 lb, was diagnosed with metastases to bone, breast cancer recurrent and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: abscess oral, blood glucose increased, excessive granulation tissue, gamma-glutamyltransferase decreased, gingival blister, gingival disorder, glycosylated haemoglobin increased, mass, oral cavity fistula, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with FEMARA, FARESTON, ARIMIDEX, AROMASIN, LEUPROLIDE ACETATE. Patient recovered.

Zometa Side Effects Report #5513737-8
ZOMETA problem was reported by a Consumer or non-health professional from JAPAN on Nov 05, 2007. Female patient, 54 years of age, weighting 105.8 lb, was diagnosed with metastases to bone, breast cancer recurrent and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: abscess oral, blood glucose increased, excessive granulation tissue, gamma-glutamyltransferase decreased, gingival blister, gingival disorder, glycosylated haemoglobin increased, mass, oral cavity fistula, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with FEMARA, FARESTON, ARIMIDEX, AROMASIN, LEUPROLIDE ACETATE. Patient recovered.

Actonel Side Effects Report #5553369-9
Physician from UNITED STATES reported ACTONEL problem on May 23, 2007. Female patient, 83 years of age, weighting 115.1 lb, was diagnosed with osteoporosis, arthralgia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abscess oral, bone erosion, excessive granulation tissue, oral candidiasis, osteonecrosis, osteosclerosis, . ACTONEL dosage: unknown. During the same period patient was treated with PREDNISONE. Patient recovered.

Zometa Side Effects Report #5489037-1
ZOMETA problem was reported by a Physician from JAPAN on Oct 10, 2007. Female patient, 54 years of age, weighting 105.8 lb, was diagnosed with metastases to bone, breast cancer recurrent and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: abscess oral, blood glucose increased, excessive granulation tissue, gamma-glutamyltransferase decreased, gingival blister, gingival disorder, glycosylated haemoglobin increased, mass, oral cavity fistula, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with FEMARA, FARESTON, ARIMIDEX, AROMASIN, LEUPROLIDE ACETATE. Patient recovered.

Zometa Side Effects Report #5495585-0
Physician from JAPAN reported ZOMETA problem on Oct 17, 2007. Female patient, 54 years of age, weighting 105.8 lb, was diagnosed with metastases to bone, breast cancer recurrent and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: abscess oral, blood glucose increased, excessive granulation tissue, gamma-glutamyltransferase decreased, gingival blister, gingival disorder, glycosylated haemoglobin increased, mass, oral cavity fistula, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with FEMARA, FARESTON, ARIMIDEX, AROMASIN, LEUPROLIDE ACETATE. Patient recovered.

Zometa Side Effects Report #5414856-7
ZOMETA problem was reported by a Consumer or non-health professional from GERMANY on Aug 10, 2007. Female patient, 64 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone disorder, bone lesion, excessive granulation tissue, histology abnormal, impaired healing, inflammation, oral surgery, osteonecrosis, tooth extraction, . ZOMETA dosage: 4 MG, QD. During the same period patient was treated with CLINDAMYCIN, QUINAPRIL, HYDROCHLOROTHIAZIDE, RANTUDIL. Patient recovered.

Zoledronic Side Effects Report #5422077-7
Physician from UNITED KINGDOM reported ZOLEDRONIC ACID problem on Aug 13, 2007. Female patient, 53 years of age, weighting 124.3 lb, was diagnosed with metastases to bone and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: abscess, bone formation decreased, excessive granulation tissue, gingival infection, osteonecrosis, tooth extraction, . ZOLEDRONIC ACID dosage: 4 MG, UNK. Patient recovered.