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Remicade Side Effects Report #5646271-5
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Feb 21, 2008. Female patient, weighting 214.0 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . REMICADE dosage: unknown. Patient recovered.

Strattera Side Effects Report #5618897-6
STRATTERA problem was reported by a Physician from GERMANY on Jan 28, 2008. Male patient, child 9 years of age, weighting 58.42 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . STRATTERA dosage: unknown. During the same period patient was treated with MEDIKINET. Patient recovered.

Primaxin Side Effects Report #5623686-2
Consumer or non-health professional from UNITED STATES reported PRIMAXIN problem on May 25, 2007. Male patient, 72 years of age, was diagnosed with pneumonia and was treated with PRIMAXIN. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . PRIMAXIN dosage: unknown. During the same period patient was treated with FIRSTCIN, CLARITHROMYCIN. Patient recovered.

Arixtra Side Effects Report #5532077-4
ARIXTRA problem was reported by a Physician from JAPAN on Nov 29, 2007. Female patient, 85 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.


Decadron Side Effects Report #5571106-9
Consumer or non-health professional from HONG KONG reported DECADRON problem on Dec 17, 2007. Female patient, 49 years of age, was diagnosed with hypersensitivity, rheumatoid arthritis and was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . DECADRON dosage: unknown. During the same period patient was treated with ELTROMBOPAG OLAMINE. Patient was hospitalized. Patient recovered.

Decadron Side Effects Report #5571112-4
DECADRON problem was reported by a Consumer or non-health professional from HONG KONG on Dec 17, 2007. Female patient, 79 years of age, was diagnosed with hypersensitivity, rheumatoid arthritis and was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . DECADRON dosage: unknown. During the same period patient was treated with GLOBULIN, VINCRISTINE SULPHATE, CYCLOSPORINE, ELTROMBOPAG OLAMINE, DANAZOL. Patient was hospitalized. Patient recovered.

Dacogen Side Effects Report #5571427-X
Health Professional from UNITED STATES reported DACOGEN problem on Dec 06, 2007. Male patient, 79 years of age, was diagnosed with myelodysplastic syndrome and was treated with DACOGEN. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . DACOGEN dosage: 32 MG, 1 IN 1 DAY, INTRAVENOUS. Patient recovered.

Chantix Side Effects Report #5572395-7
CHANTIX problem was reported by a Pharmacist from UNITED STATES on Dec 11, 2007. Female patient, weighting 159.4 lb, was diagnosed with sinus congestion, ulcer, chronic obstructive pulmonary disease, blood cholesterol and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: platelet count increased, pneumonia, . CHANTIX dosage: unknown. During the same period patient was treated with MUCINEX, PROTONIX, MONTELUKAST, ZETIA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5504193-4
Pharmacist from JAPAN reported ARIXTRA problem on Oct 29, 2007. Male patient, 55 years of age, weighting 132.5 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with MEROPEN, LACTEC, LOXOPROFEN, MUCOSTA. Patient recovered.


Anagrelide Side Effects Report #5522873-1
ANAGRELIDE HCI problem was reported by a Pharmacist from UNITED STATES on Nov 02, 2007. Female patient, 84 years of age, was diagnosed with thrombocythaemia and was treated with ANAGRELIDE HCI. After drug was administered, patient experienced the following problems/side effects: platelet count increased, transient ischaemic attack, . ANAGRELIDE HCI dosage: 3 MG, QD, ORAL. During the same period patient was treated with ASPIRIN, CALCIUM, DILTIAZEM, JANUMET, LEVOTHYROXINE, PAXIL, PLAVIX. Patient was hospitalized. Patient recovered.

Flagyl Side Effects Report #5524309-3
Consumer or non-health professional from UNITED STATES reported FLAGYL problem on Nov 13, 2007. Male patient, child 7 years of age, weighting 50.04 lb, was diagnosed with giardiasis, typhoid fever and was treated with FLAGYL. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . FLAGYL dosage: unknown. During the same period patient was treated with ROCEPHIN, BACTRIM, MOTRIN. Patient recovered.

Dacogen Side Effects Report #5525328-3
DACOGEN problem was reported by a Health Professional from UNITED STATES on Nov 05, 2007. Female patient was treated with DACOGEN. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . DACOGEN dosage: unknown. Patient recovered.

Forteo Side Effects Report #5526517-4
Physician from BELGIUM reported FORTEO problem on Nov 12, 2007. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . FORTEO dosage: unknown. Patient recovered.

Arixtra Side Effects Report #5527337-7
ARIXTRA problem was reported by a Physician from JAPAN on Nov 22, 2007. Female patient, 69 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.


Arixtra Side Effects Report #5474801-5
Pharmacist from JAPAN reported ARIXTRA problem on Oct 01, 2007. Male patient, 55 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . ARIXTRA dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Topamax Side Effects Report #5480644-9
TOPAMAX problem was reported by a Consumer or non-health professional from CHINA on Sept 28, 2007. Male patient, 50 years of age, was diagnosed with epilepsy, myocardial ischaemia and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: platelet count increased, rash, . TOPAMAX dosage: unknown. During the same period patient was treated with ANTIEPILEPSIRINE, ISOSORBIDE MONONITRATE. Patient was hospitalized. Patient recovered.

Topamax Side Effects Report #5490594-X
Consumer or non-health professional from CHINA reported TOPAMAX problem on Oct 10, 2007. Male patient, 50 years of age, was diagnosed with epilepsy, myocardial infarction and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: platelet count increased, rash, . TOPAMAX dosage: unknown. During the same period patient was treated with ANTIEPILEPSIRINE, ISOSORBIDE MONONITRATE. Patient was hospitalized. Patient recovered.

Zyprexa Side Effects Report #5441460-7
ZYPREXA problem was reported by a Physician from GERMANY on Aug 23, 2007. Male patient, 40 years of age, was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, white blood cell count increased, . ZYPREXA dosage: unknown. During the same period patient was treated with TAVOR. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5404004-1
Physician from GERMANY reported ARIXTRA problem on July 30, 2007. Male patient, 56 years of age, was diagnosed with thrombosis prophylaxis, pain and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, thrombocythaemia, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with TRAMAL LONG, IBUHEXAL, PANTOPRAZOLE, NOVALGIN. Patient recovered.


Avastin Side Effects Report #5410190-X
AVASTIN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 02, 2007. Female patient, weighting 192.0 lb, was diagnosed with ovarian cancer and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . AVASTIN dosage: 1300 MG, Q4W. During the same period patient was treated with GEMZAR. Patient recovered.

Trombyl Side Effects Report #5427469-8
Consumer or non-health professional from SWEDEN reported TROMBYL problem on Aug 21, 2007. Male patient, 82 years of age, was diagnosed with blood potassium increased and was treated with TROMBYL. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . TROMBYL dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE, PLENDIL, ATACAND, HYDREA, ESIDRIX. Patient recovered.

Trombyl Side Effects Report #5428789-3
TROMBYL problem was reported by a Consumer or non-health professional from SWEDEN on Aug 21, 2007. Male patient, 82 years of age, was diagnosed with blood potassium increased and was treated with TROMBYL. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . TROMBYL dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE, PLENDIL, ATACAND, HYDREA, ESIDRIX. Patient recovered.

Procrit Side Effects Report #5396839-9
Pharmacist from UNITED STATES reported PROCRIT problem on Aug 23, 2006. Female patient, weighting 180.8 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . PROCRIT dosage: unknown. During the same period patient was treated with VITAMIN B, HEPARIN, CELEBREX, HYDROCHLOROTHIAZIDE. Patient recovered.

Procrit Side Effects Report #5398643-4
PROCRIT problem was reported by a Health Professional from UNITED STATES on May 18, 2007. Female patient, weighting 130.1 lb, was diagnosed with myelodysplastic syndrome and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: platelet count increased, therapeutic response decreased, . PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5396839-9
Pharmacist from UNITED STATES reported PROCRIT problem on Aug 23, 2006. Female patient, weighting 180.8 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . PROCRIT dosage: unknown. During the same period patient was treated with VITAMIN B, HEPARIN, CELEBREX, HYDROCHLOROTHIAZIDE. Patient recovered.

Procrit Side Effects Report #5398643-4
PROCRIT problem was reported by a Health Professional from UNITED STATES on May 18, 2007. Female patient, weighting 130.1 lb, was diagnosed with myelodysplastic syndrome and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: platelet count increased, therapeutic response decreased, . PROCRIT dosage: unknown. Patient recovered.

Humira Side Effects Report #5769054-4
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Mar 18, 2008. Male patient, weighting 118.1 lb, was diagnosed with crohn's disease, mineral supplementation and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . HUMIRA dosage: unknown. During the same period patient was treated with IRON SUPPLEMENT, CALCIUM, MESALAMINE. Patient recovered.

Byetta Side Effects Report #5799744-9
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Male patient, 75 years of age, weighting 198.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with AMARYL. Patient recovered.

Abciximab Side Effects Report #5728675-5
Physician from GERMANY reported ABCIXIMAB problem on Apr 29, 2008. Male patient, 48 years of age, was diagnosed with myocardial infarction and was treated with ABCIXIMAB. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . ABCIXIMAB dosage: unknown. Patient recovered.

Abciximab Side Effects Report #5737844-X
ABCIXIMAB problem was reported by a Physician from GERMANY on May 08, 2008. Male patient, 48 years of age, was diagnosed with myocardial infarction and was treated with ABCIXIMAB. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . ABCIXIMAB dosage: unknown. During the same period patient was treated with ASPIRIN, CLOPIDOGREL. Patient recovered.

Strattera Side Effects Report #5740812-5
Physician from GERMANY reported STRATTERA problem on May 06, 2008. Male patient, child 9 years of age, weighting 58.42 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . STRATTERA dosage: unknown. During the same period patient was treated with MEDIKINET. Patient recovered.

Yasmin Side Effects Report #5696631-1
YASMIN problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 22, 2006. Female patient, 25 years of age, was diagnosed with oral contraception and was treated with YASMIN. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . YASMIN dosage: unknown. Patient recovered.

Climara Side Effects Report #5715578-5
Consumer or non-health professional from UNITED STATES reported CLIMARA problem on Apr 15, 2008. Female patient, 46 years of age, was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, thrombocythaemia, . CLIMARA dosage: unknown. Patient recovered.

Zoloft Side Effects Report #5351138-6
ZOLOFT problem was reported by a Consumer or non-health professional from SWEDEN on May 30, 2007. Female patient, 41 years of age, was diagnosed with depression, fatigue and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: platelet count increased, streptococcal infection, . ZOLOFT dosage: unknown. During the same period patient was treated with ZOLPIDEM, DULOXETINE. Patient recovered.

Cisplatin Side Effects Report #5320309-7
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on May 09, 2007. Male patient, 71 years of age, was diagnosed with gastric cancer, abdominal pain, prophylaxis, varicose vein, hypertension and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: platelet count increased, tumour haemorrhage, vomiting, . CISPLATIN dosage: unknown. During the same period patient was treated with MORPHINE SULPHATE, OMEPRAZOLE, ESBERIVEN, COZAAR. Patient was hospitalized. Patient recovered.

Trileptal Side Effects Report #5321002-7
TRILEPTAL problem was reported by a Consumer or non-health professional from BRAZIL on Apr 30, 2007. Female patient was diagnosed with convulsion and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . TRILEPTAL dosage: 300 MG, Q8H. Patient recovered.

Trileptal Side Effects Report #5322441-0
Consumer or non-health professional from BRAZIL reported TRILEPTAL problem on Apr 30, 2007. Female patient was diagnosed with convulsion and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . TRILEPTAL dosage: 300 MG, Q8H. Patient recovered.

Crestor Side Effects Report #5328892-2
CRESTOR problem was reported by a Physician from JAPAN on May 09, 2007. Female patient, weighting 123.5 lb, was diagnosed with hyperlipidaemia, gastric ulcer, acute myocardial infarction, cardiac failure congestive and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . CRESTOR dosage: unknown. During the same period patient was treated with OMEPRAL, SIGMART, ASPIRIN, TICLOPIDINE, LASIX, ALDACTONE. Patient was hospitalized. Patient recovered.

Gemzar Side Effects Report #5330846-7
Physician from UNITED STATES reported GEMZAR problem on May 11, 2007. Female patient, 51 years of age, was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . GEMZAR dosage: 1350 MG, UNK. During the same period patient was treated with TAXOTERE, ZOMETA. Patient recovered.

Gemzar Side Effects Report #5333632-7
GEMZAR problem was reported by a Physician from UNITED STATES on May 11, 2007. Female patient, 51 years of age, was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, radiation skin injury, . GEMZAR dosage: 1350 MG, UNK. During the same period patient was treated with TAXOTERE, ZOMETA. Patient recovered.

Zoloft Side Effects Report #5340500-3
Consumer or non-health professional from SWEDEN reported ZOLOFT problem on May 22, 2007. Female patient, 41 years of age, was diagnosed with depression, fatigue and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: platelet count increased, uterine inflammation, . ZOLOFT dosage: unknown. During the same period patient was treated with ZOLPIDEM. Patient recovered.

Gemzar Side Effects Report #5290330-6
GEMZAR problem was reported by a Physician from JAPAN on Mar 28, 2007. Male patient, 71 years of age, weighting 90.39 lb, was diagnosed with malignant neoplasm of renal pelvis and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . GEMZAR dosage: 1200 MG, OTHER. During the same period patient was treated with RANDA. Patient recovered.

Gemzar Side Effects Report #5293006-4
Physician from IRELAND reported GEMZAR problem on Mar 30, 2007. Female patient was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . GEMZAR dosage: unknown. Patient recovered.

Gemzar Side Effects Report #5293013-1
GEMZAR problem was reported by a Physician from IRELAND on Mar 30, 2007. Male patient was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . GEMZAR dosage: unknown. Patient recovered.

Lipitor Side Effects Report #5293917-X
Physician from UNITED STATES reported LIPITOR problem on Mar 30, 2007. Male patient, 60 years of age, was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . LIPITOR dosage: unknown. Patient recovered.

Hydrea Side Effects Report #5306060-8
HYDREA problem was reported by a Consumer or non-health professional from UNITED STATES on June 08, 2006. Female patient, 87 years of age, weighting 152.1 lb, was diagnosed with essential thrombocythaemia and was treated with HYDREA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, red blood cell count increased, white blood cell count decreased, . HYDREA dosage: unknown. During the same period patient was treated with SYNTHROID, COZAAR, CALCIUM. Patient recovered.

Cymbalta Side Effects Report #5341213-4
Physician from UNITED STATES reported CYMBALTA problem on Nov 27, 2006. Female patient, 42 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: platelet count increased, red blood cell abnormality, . CYMBALTA dosage: unknown. During the same period patient was treated with WELLBUTRIN. Patient recovered.

Crestor Side Effects Report #5239009-7
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on June 15, 2005. Female patient, 68 years of age, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, platelet disorder, . CRESTOR dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Gemzar Side Effects Report #5270262-X
Physician from JAPAN reported GEMZAR problem on Mar 12, 2007. Male patient, 71 years of age, was diagnosed with malignant neoplasm of renal pelvis and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . GEMZAR dosage: 1200 MG, OTHER. During the same period patient was treated with RANDA. Patient recovered.

Clozaril Side Effects Report #5284822-3
CLOZARIL problem was reported by a Physician from UNITED STATES on May 16, 2006. Male patient, 45 years of age, was diagnosed with schizophrenia and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: platelet count increased, . CLOZARIL dosage: unknown. During the same period patient was treated with ABILIFY. Patient recovered.

Epogen Side Effects Report #5664332-1
Physician from UNITED STATES reported EPOGEN problem on Feb 29, 2008. Female patient, 31 years of age, was diagnosed with renal failure chronic and was treated with EPOGEN. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, platelet count increased, pneumonia klebsiella, pneumonia staphylococcal, therapeutic response decreased, white blood cell count increased, . EPOGEN dosage: unknown. During the same period patient was treated with ARANESP, LINEZOLID, IMIPENEM, TOBRAMYCIN, LISINOPRIL, METOPROLOL TARTRATE, CLONIDINE, SYNTHROID. Patient was hospitalized. Patient recovered.