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TUMOUR MARKER INCREASED side effect

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Sortis Side Effects Report #5620808-4
Consumer or non-health professional from GERMANY reported SORTIS problem on Jan 31, 2008. Female patient, 61 years of age, was diagnosed with hypercholesterolaemia and was treated with SORTIS. After drug was administered, patient experienced the following problems/side effects: tumour marker increased, . SORTIS dosage: unknown. Patient recovered.

Sortis Side Effects Report #5606780-1
SORTIS problem was reported by a Consumer or non-health professional from GERMANY on Jan 18, 2008. Female patient, 61 years of age, was diagnosed with hypercholesterolaemia and was treated with SORTIS. After drug was administered, patient experienced the following problems/side effects: tumour marker increased, . SORTIS dosage: unknown. Patient recovered.

Arimidex Side Effects Report #5528164-7
Consumer or non-health professional from BRAZIL reported ARIMIDEX problem on Nov 19, 2007. Female patient, 59 years of age, weighting 154.3 lb, was diagnosed with metastases to bone and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: tumour marker increased, . ARIMIDEX dosage: unknown. Patient recovered.

Tykerb Side Effects Report #5482553-8
TYKERB problem was reported by a Health Professional from UNITED STATES on June 28, 2007. Female patient was treated with TYKERB. After drug was administered, patient experienced the following problems/side effects: tumour marker increased, . TYKERB dosage: 5MG PER DAY. Patient recovered.


Herceptin Side Effects Report #5759300-5
Physician from UNITED KINGDOM reported HERCEPTIN problem on May 20, 2008. Female patient was diagnosed with breast cancer and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: tumour marker increased, . HERCEPTIN dosage: unknown. Patient recovered.

Boniva Side Effects Report #5604473-8
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 18, 2008. Female patient, 52 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: influenza like illness, tumour marker increased, . BONIVA dosage: unknown. During the same period patient was treated with FEMARA. Patient recovered.

Omeprazole Side Effects Report #5565077-9
Health Professional from HUNGARY reported OMEPRAZOLE problem on Dec 10, 2007. Female patient, 73 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with OMEPRAZOLE. After drug was administered, patient experienced the following problems/side effects: enterochromaffin cell hyperplasia, tumour marker increased, . OMEPRAZOLE dosage: unknown. During the same period patient was treated with LANSOPRAZOLE. Patient recovered.

Lyrica Side Effects Report #5490997-3
LYRICA problem was reported by a Pharmacist from GERMANY on Oct 10, 2007. Female patient was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: oral discomfort, tumour marker increased, . LYRICA dosage: DAILY DOSE:75MG. Patient recovered.

Lyrica Side Effects Report #5389572-0
Pharmacist from GERMANY reported LYRICA problem on July 07, 2007. Female patient was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: oral discomfort, tumour marker increased, . LYRICA dosage: DAILY DOSE:75MG. Patient recovered.


Lyrica Side Effects Report #5389572-0
LYRICA problem was reported by a Pharmacist from GERMANY on July 07, 2007. Female patient was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: oral discomfort, tumour marker increased, . LYRICA dosage: DAILY DOSE:75MG. Patient recovered.

Clozapine Side Effects Report #5284271-8
Physician from GERMANY reported CLOZAPINE problem on Mar 21, 2007. Female patient was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: breast cancer, tumour marker increased, . CLOZAPINE dosage: UP TO 100 MG, QD. During the same period patient was treated with VENLAFAXINE. Patient recovered.

Forteo Side Effects Report #5292233-X
FORTEO problem was reported by a Consumer or non-health professional from SPAIN on Mar 27, 2007. Female patient, 55 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: pulmonary thrombosis, tumour marker increased, . FORTEO dosage: unknown. During the same period patient was treated with EVISTA. Patient recovered.

Iressa Side Effects Report #5264514-7
Consumer or non-health professional from UNITED STATES reported IRESSA problem on Dec 27, 2004. Female patient, 67 years of age, was diagnosed with non-small cell lung cancer and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: cardiac disorder, tumour marker increased, . IRESSA dosage: unknown. Patient recovered.

Arimidex Side Effects Report #5675189-7
ARIMIDEX problem was reported by a Health Professional from BRAZIL on Mar 13, 2008. Female patient, 68 years of age, weighting 183.0 lb, was diagnosed with breast cancer, hypertension and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, fatigue, tumour marker increased, . ARIMIDEX dosage: unknown. During the same period patient was treated with FASLODEX, HERCEPTIN, MODURETIC, RENITEC. Patient recovered.


Tykerb Side Effects Report #5588383-0
Consumer or non-health professional from UNITED STATES reported TYKERB problem on Oct 29, 2007. Female patient, 43 years of age, was diagnosed with breast cancer and was treated with TYKERB. After drug was administered, patient experienced the following problems/side effects: ill-defined disorder, tumour marker increased, . TYKERB dosage: 1250MG PER DAY. During the same period patient was treated with FASLODEX, XELODA. Patient recovered.

Revlimid Side Effects Report #5645782-6
REVLIMID problem was reported by a Health Professional from UNITED STATES on Dec 12, 2007. Female patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: bone pain, neoplasm progression, tumour marker increased, white blood cell count decreased, . REVLIMID dosage: 20 MG, 2 IN 1 D, ORAL; 10 MG, DAILY X 21 DAYS, ORAL 5MG-10MG, DAILY, ORAL. Patient recovered.

Arimidex Side Effects Report #5415299-2
Consumer or non-health professional from UNITED STATES reported ARIMIDEX problem on Aug 10, 2007. Female patient, 55 years of age, weighting 203.0 lb, was diagnosed with breast cancer stage iv and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: joint sprain, pulmonary embolism, tumour marker increased, . ARIMIDEX dosage: unknown. During the same period patient was treated with ZOMETA, FASLODEX. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5422237-5
ENBREL problem was reported by a Consumer or non-health professional from SPAIN on Aug 13, 2007. Female patient, 56 years of age, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: carbohydrate antigen 125 increased, carcinoembryonic antigen increased, tumour marker increased, . ENBREL dosage: unknown. Patient recovered.

Arimidex Side Effects Report #5691799-5
Consumer or non-health professional from BRAZIL reported ARIMIDEX problem on Mar 27, 2008. Female patient, 59 years of age, weighting 154.3 lb, was diagnosed with metastases to bone, breast cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: endometrial hypertrophy, metastases to bone, tumour marker increased, . ARIMIDEX dosage: unknown. During the same period patient was treated with TAMOXIFEN CITRATE, PURAN T, LORAX, NAZEDRON. Patient recovered.


Topotecan Side Effects Report #5697710-5
TOPOTECAN problem was reported by a Physician from GERMANY on Apr 04, 2008. Female patient, 55 years of age, weighting 180.8 lb, was treated with TOPOTECAN. After drug was administered, patient experienced the following problems/side effects: metastases to spleen, metastatic neoplasm, tumour marker increased, . TOPOTECAN dosage: 1.25MG CYCLIC. Patient was hospitalized. Patient recovered.

Zofran Side Effects Report #5719890-5
Consumer or non-health professional from UNITED STATES reported ZOFRAN problem on July 24, 2007. Female patient, 56 years of age, was diagnosed with prophylaxis of nausea and vomiting and was treated with ZOFRAN. After drug was administered, patient experienced the following problems/side effects: nausea, tumour marker increased, weight decreased, . ZOFRAN dosage: 8MG THREE TIMES PER DAY. During the same period patient was treated with XELODA, PROTONIX, PANCREATIC ENZYMES. Patient recovered.

Faslodex Side Effects Report #5360051-X
FASLODEX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 18, 2006. Female patient, 49 years of age, weighting 154.1 lb, was diagnosed with breast cancer female and was treated with FASLODEX. After drug was administered, patient experienced the following problems/side effects: myalgia, nausea, tumour marker increased, . FASLODEX dosage: unknown. During the same period patient was treated with ZOMETTA, TAMOXIFEN CITRATE, ARIMIDEX. Patient recovered.

Arimidex Side Effects Report #5314809-3
Consumer or non-health professional from UNITED STATES reported ARIMIDEX problem on Apr 27, 2007. Female patient, 55 years of age, weighting 203.0 lb, was diagnosed with breast cancer stage iv and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: joint sprain, pulmonary embolism, tumour marker increased, . ARIMIDEX dosage: unknown. During the same period patient was treated with ZOMETA, FASLODEX. Patient was hospitalized. Patient recovered.

Symlin Side Effects Report #5324901-5
SYMLIN problem was reported by a Physician from UNITED STATES on Apr 25, 2007. Male patient was treated with SYMLIN. After drug was administered, patient experienced the following problems/side effects: hepatic enzyme increased, jaundice, tumour marker increased, . SYMLIN dosage: unknown. Patient was hospitalized. Patient recovered.

Symlin Side Effects Report #5325445-7
Physician from UNITED STATES reported SYMLIN problem on Apr 25, 2007. Male patient was treated with SYMLIN. After drug was administered, patient experienced the following problems/side effects: hepatic enzyme increased, jaundice, tumour marker increased, . SYMLIN dosage: unknown. Patient was hospitalized. Patient recovered.

Iressa Side Effects Report #5264513-5
IRESSA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 28, 2004. Female patient, 68 years of age, weighting 148.0 lb, was diagnosed with non-small cell lung cancer and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: alopecia, lung infiltration, tumour marker increased, . IRESSA dosage: unknown. During the same period patient was treated with OXYCONTIN, NEURONTIN, ACTONEL. Patient recovered.

Iressa Side Effects Report #5265479-4
Consumer or non-health professional from UNITED STATES reported IRESSA problem on Sept 13, 2004. Male patient, 65 years of age, weighting 202.0 lb, was diagnosed with non-small cell lung cancer and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: dermatitis exfoliative, dry skin, tumour marker increased, . IRESSA dosage: unknown. During the same period patient was treated with AVANDIA, COREG. Patient recovered.

Iressa Side Effects Report #5265771-3
IRESSA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 28, 2004. Female patient, 68 years of age, weighting 148.0 lb, was diagnosed with non-small cell lung cancer and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: alopecia, lung infiltration, tumour marker increased, . IRESSA dosage: unknown. During the same period patient was treated with OXYCONTIN, NEURONTIN, ACTONEL. Patient recovered.