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Aleve Side Effects Report #5658567-1
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Mar 08, 2007. Male patient, 75 years of age, weighting 249.1 lb, was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with LOTREL, ATENOLOL, LIPITOR, ADVAIR DISKUS, ALBUTEROL INHALERS. Patient recovered.

Aranesp Side Effects Report #5684041-2
ARANESP problem was reported by a Consumer or non-health professional from GERMANY on Mar 17, 2008. Female patient, 81 years of age, was diagnosed with renal failure chronic and was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, injection site pain, international normalised ratio increased, sleep disorder, . ARANESP dosage: unknown. During the same period patient was treated with MARCUMAR. Patient recovered.

Enbrel Side Effects Report #5610829-X
Health Professional from JAPAN reported ENBREL problem on Jan 18, 2008. Female patient, weighting 68.34 lb, was diagnosed with rheumatoid arthritis, gastric ulcer, hyperuricaemia, abdominal distension, osteoporosis, constipation and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, lung infection, thrombocytopenia, . ENBREL dosage: unknown. During the same period patient was treated with PREDNISOLONE, PROMAC, ALLOPURINOL, GASCON, ALENDRONATE, ALOSENN. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5624560-8
ENBREL problem was reported by a Health Professional from JAPAN on Jan 30, 2008. Female patient, weighting 68.34 lb, was diagnosed with rheumatoid arthritis, gastric ulcer, hyperuricaemia, abdominal distension, osteoporosis, constipation and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, lung infection, thrombocytopenia, . ENBREL dosage: unknown. During the same period patient was treated with PREDNISOLONE, PROMAC, ZYLORIC, GASCON, ALENDRONATE, ALOSENN. Patient was hospitalized. Patient recovered.


Prednisolone Side Effects Report #5642057-6
Health Professional from UNITED STATES reported PREDNISOLONE problem on Feb 15, 2008. Female patient, weighting 68.34 lb, was diagnosed with rheumatoid arthritis, gastric ulcer and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, immunosuppression, lung infection, marrow hyperplasia, melaena, thrombocytopenia, . PREDNISOLONE dosage: DAILY DOSE:15MG-FREQ:QD. During the same period patient was treated with ETANERCEPT, PROMAC. Patient was hospitalized. Patient recovered.

Escitalopram Side Effects Report #5646206-5
ESCITALOPRAM problem was reported by a Consumer or non-health professional from SWEDEN on Feb 12, 2008. Male patient, 54 years of age, was diagnosed with depression, thrombosis prophylaxis and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, obesity, post procedural haemorrhage, . ESCITALOPRAM dosage: 25 MG QD PO. During the same period patient was treated with ENOXAPARIN, OMEGA, VENTOLIN, PULMICORT. Patient was hospitalized. Patient recovered.

Novolog Side Effects Report #5599964-2
Physician from JAPAN reported NOVOLOG problem on Jan 15, 2008. Female patient, weighting 143.3 lb, was diagnosed with insulin-requiring type 2 diabetes mellitus and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, hepatic cirrhosis, idiopathic thrombocytopenic purpura, . NOVOLOG dosage: unknown. During the same period patient was treated with LANIRAPID, URSO, PREDNISOLONE, LENDORMIN, FUROSEMIDE, WARFARIN, BAKTAR, TAKEPRON. Patient was hospitalized. Patient recovered.

Plavix Side Effects Report #5621205-8
PLAVIX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 13, 2006. Female patient was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . PLAVIX dosage: unknown. Patient was hospitalized. Patient recovered.

Casodex Side Effects Report #5531767-7
Physician from JAPAN reported CASODEX problem on Nov 22, 2007. Male patient, 74 years of age, was diagnosed with prostate cancer and was treated with CASODEX. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, malaise, . CASODEX dosage: unknown. During the same period patient was treated with LENDORMIN, LEUPROLIDE ACETATE, LEUPLIN. Patient was hospitalized. Patient recovered.


Voltaren Side Effects Report #5562743-6
VOLTAREN problem was reported by a Physician from JAPAN on Dec 07, 2007. Male patient, 57 years of age, was diagnosed with spinal osteoarthritis and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . VOLTAREN dosage: 75 MG/DAY. During the same period patient was treated with ATELEC, LENDORMIN. Patient recovered.

Pegasys Side Effects Report #5507894-7
Physician from JAPAN reported PEGASYS problem on Oct 25, 2007. Male patient, 60 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . PEGASYS dosage: unknown. Patient recovered.

Pegasys Side Effects Report #5488252-0
PEGASYS problem was reported by a Physician from JAPAN on Oct 05, 2007. Male patient, 60 years of age, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . PEGASYS dosage: unknown. Patient recovered.

Zyvox Side Effects Report #5471790-4
Physician from JAPAN reported ZYVOX problem on Sept 18, 2007. Male patient, weighting 105.8 lb, was diagnosed with staphylococcal infection, pneumonia staphylococcal, convulsion and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, platelet count decreased, . ZYVOX dosage: unknown. During the same period patient was treated with DEPAKENE, TARGOCID. Patient was hospitalized. Patient recovered.

Diflucan Side Effects Report #5414250-9
DIFLUCAN problem was reported by a Physician from EGYPT on Aug 06, 2007. Male patient, weighting 7.72 lb, was diagnosed with oral candidiasis and was treated with DIFLUCAN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . DIFLUCAN dosage: unknown. During the same period patient was treated with VITAMIN CAP. Patient died on 08/05/2007.


Enbrel Side Effects Report #5380997-6
Health Professional from AUSTRIA reported ENBREL problem on June 29, 2007. Female patient, weighting 143.3 lb, was diagnosed with polyarthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, injection site oedema, injection site pruritus, skin fissures, . ENBREL dosage: unknown. During the same period patient was treated with ELOCON, SYMBICORT, IBUPROFEN, PROXEN. Patient recovered.

Ambisome Side Effects Report #5383182-7
AMBISOME problem was reported by a Physician from FINLAND on June 22, 2007. Male patient was diagnosed with fungal infection and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, hypokalaemia, impaired healing, neonatal disorder, oliguria, respiratory disorder, skin necrosis, thrombocytopenia, . AMBISOME dosage: 7 MG/KG, UID/QD, UNK. During the same period patient was treated with FLUCONAZOLE, AMPICILLIN, GENTAMICIN, METRONIDAZOLE, OMEPRAZOLE. Patient recovered.

Tazocin Side Effects Report #5392479-6
Health Professional from DENMARK reported TAZOCIN problem on July 19, 2007. Male patient, weighting 194.0 lb, was diagnosed with infection and was treated with TAZOCIN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, mucosal haemorrhage, skin haemorrhage, . TAZOCIN dosage: unknown. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5380997-6
ENBREL problem was reported by a Health Professional from AUSTRIA on June 29, 2007. Female patient, weighting 143.3 lb, was diagnosed with polyarthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, injection site oedema, injection site pruritus, skin fissures, . ENBREL dosage: unknown. During the same period patient was treated with ELOCON, SYMBICORT, IBUPROFEN, PROXEN. Patient recovered.

Ambisome Side Effects Report #5383182-7
Physician from FINLAND reported AMBISOME problem on June 22, 2007. Male patient was diagnosed with fungal infection and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, hypokalaemia, impaired healing, neonatal disorder, oliguria, respiratory disorder, skin necrosis, thrombocytopenia, . AMBISOME dosage: 7 MG/KG, UID/QD, UNK. During the same period patient was treated with FLUCONAZOLE, AMPICILLIN, GENTAMICIN, METRONIDAZOLE, OMEPRAZOLE. Patient recovered.


Tazocin Side Effects Report #5392479-6
TAZOCIN problem was reported by a Health Professional from DENMARK on July 19, 2007. Male patient, weighting 194.0 lb, was diagnosed with infection and was treated with TAZOCIN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, mucosal haemorrhage, skin haemorrhage, . TAZOCIN dosage: unknown. Patient was hospitalized. Patient recovered.

Hyzaar Side Effects Report #5759273-5
Physician from JAPAN reported HYZAAR problem on May 29, 2008. Male patient, 60 years of age, weighting 194.0 lb, was diagnosed with hypertension and was treated with HYZAAR. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . HYZAAR dosage: unknown. During the same period patient was treated with OLMETEC, LIPITOR, NORVASC, ALLOPURINOL. Patient recovered.

Aranesp Side Effects Report #5734496-X
ARANESP problem was reported by a Consumer or non-health professional from GERMANY on Apr 30, 2008. Female patient, 81 years of age, was diagnosed with renal failure chronic and was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, injection site pain, international normalised ratio increased, osteoarthritis, sleep disorder, . ARANESP dosage: unknown. During the same period patient was treated with MARCUMAR. Patient recovered.

Zyban Side Effects Report #5719618-9
Consumer or non-health professional from DENMARK reported ZYBAN problem on Apr 24, 2008. Male patient, 51 years of age, weighting 138.9 lb, was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . ZYBAN dosage: 300MG PER DAY. Patient recovered.

Meropen Side Effects Report #5344311-4
MEROPEN problem was reported by a Health Professional from JAPAN on May 23, 2007. Female patient, 57 years of age, weighting 242.5 lb, was diagnosed with meningitis bacterial, dehydration, depressed level of consciousness and was treated with MEROPEN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, vitamin k deficiency, . MEROPEN dosage: unknown. During the same period patient was treated with VICCILLIN, SOLITA T, NICOLIN. Patient was hospitalized. Patient recovered.

Meropen Side Effects Report #5349251-2
Health Professional from JAPAN reported MEROPEN problem on June 04, 2007. Female patient, 57 years of age, weighting 242.5 lb, was diagnosed with meningitis bacterial, dehydration, depressed level of consciousness and was treated with MEROPEN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, vitamin k deficiency, . MEROPEN dosage: unknown. During the same period patient was treated with VICCILLIN, SOLITA T, NICOLIN, ROCEPHIN. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5362554-0
LYRICA problem was reported by a Consumer or non-health professional from NETHERLANDS on June 07, 2007. Male patient, weighting 224.9 lb, was diagnosed with neuropathy peripheral and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . LYRICA dosage: unknown. During the same period patient was treated with METFORMIN, PARIET, RENITEC, AMLODIPINE, TRIAMTERENE, PRAVASTATIN. Patient recovered.

Paxil Side Effects Report #5363617-6
Pharmacist from JAPAN reported PAXIL problem on June 19, 2007. Female patient, 97 years of age, was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . PAXIL dosage: unknown. Patient recovered.

Lyrica Side Effects Report #5372623-7
LYRICA problem was reported by a Physician from NETHERLANDS on June 15, 2007. Male patient, weighting 224.9 lb, was diagnosed with neuropathy peripheral and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . LYRICA dosage: unknown. During the same period patient was treated with METFORMIN, PARIET, RENITEC, AMLODIPINE, TRIAMTERENE, PRAVASTATIN, INSULIN. Patient recovered.

Paxil Side Effects Report #5373545-8
Pharmacist from JAPAN reported PAXIL problem on June 22, 2007. Female patient, 97 years of age, was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . PAXIL dosage: 10MG PER DAY. During the same period patient was treated with ADALAT, TAKEPRON, BIOFERMIN R, GASMOTIN, CARNACULIN, EURODIN. Patient recovered.

Meropenem Side Effects Report #5327415-1
MEROPENEM problem was reported by a Health Professional from JAPAN on May 14, 2007. Female patient, weighting 242.5 lb, was treated with MEROPENEM. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, vitamin k deficiency, . MEROPENEM dosage: unknown. Patient recovered.

Ambisome Side Effects Report #5339346-1
Physician from FINLAND reported AMBISOME problem on May 15, 2007. Male patient, 37 years of age, was diagnosed with fungal infection and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, hypokalaemia, oliguria, respiratory disorder, skin necrosis, thrombocytopenia, . AMBISOME dosage: 7 MG/KG, UID/QD. During the same period patient was treated with FLUCONAZOLE, AMPICILLIN, GENTAMICIN, METRONIDAZOLE, OMEPRAZOLE. Patient recovered.

Byetta Side Effects Report #5364699-8
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2007. Female patient, 57 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, hypertension, injection site haemorrhage, stomach discomfort, . BYETTA dosage: unknown. During the same period patient was treated with ASPIRIN. Patient recovered.

Diflucan Side Effects Report #5267705-4
Physician from JAPAN reported DIFLUCAN problem on Mar 06, 2007. Female patient, weighting 123.5 lb, was diagnosed with fungaemia, cerebral infarction and was treated with DIFLUCAN. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . DIFLUCAN dosage: DAILY DOSE:100MG-FREQ:FREQUENCY: QD. During the same period patient was treated with PRODIF, VFEND, WARFARIN, LIVALO, DIAMOX, CARDENALIN, ALLOPURINOL, DIART. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5281670-5
GLEEVEC problem was reported by a Physician from JAPAN on Mar 16, 2007. Male patient, 55 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: haemorrhagic diathesis, thrombocytopenia, . GLEEVEC dosage: 400 MG/DAY. Patient recovered.

Aspirin Side Effects Report #5661104-9
Consumer or non-health professional from UNITED STATES reported ASPIRIN problem on Mar 03, 2008. Male patient, 55 years of age, was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: haemorrhage, haemorrhagic diathesis, . ASPIRIN dosage: unknown. Patient recovered.

Heparin Side Effects Report #5671056-3
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Female patient, 18 years of age, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: contusion, haemorrhagic diathesis, pain, tachycardia, . HEPARIN dosage: unknown. Patient recovered.

Effexor Side Effects Report #5676574-X
Physician from UNITED STATES reported EFFEXOR problem on Mar 21, 2008. Female patient, 35 years of age, was diagnosed with depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: contusion, haemorrhagic diathesis, . EFFEXOR dosage: unknown. Patient recovered.

Advate Side Effects Report #5643889-0
ADVATE problem was reported by a Health Professional from SWEDEN on Feb 21, 2008. Male patient, 57 years of age, was diagnosed with polycythaemia and was treated with ADVATE. After drug was administered, patient experienced the following problems/side effects: haemorrhagic diathesis, . ADVATE dosage: unknown. Patient recovered.

Kogenate Side Effects Report #5578843-0
Health Professional from UNITED KINGDOM reported KOGENATE problem on Nov 30, 2007. Male patient, 40 years of age, was diagnosed with factor viii deficiency and was treated with KOGENATE. After drug was administered, patient experienced the following problems/side effects: factor viii inhibition, haemorrhagic diathesis, . KOGENATE dosage: unknown. Patient recovered.

Aptivus Side Effects Report #5585082-6
APTIVUS problem was reported by a Consumer or non-health professional from on Jan 02, 2008. Male patient, 31 years of age, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic diathesis, soft tissue haemorrhage, . APTIVUS dosage: TIPRANAVIR 1000 MG/RITONAVIR 400 MG. Patient recovered.

Aptivus Side Effects Report #5585088-7
Consumer or non-health professional from reported APTIVUS problem on Jan 02, 2008. Male patient, 27 years of age, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic diathesis, injection site bruising, injection site haematoma, soft tissue haemorrhage, . APTIVUS dosage: TIPRANAVIR 1000 MG/RITONAVIR 400 MG. During the same period patient was treated with FUZEON. Patient recovered.

Aptivus Side Effects Report #5585948-7
APTIVUS problem was reported by a Consumer or non-health professional from on Jan 02, 2008. Male patient, 27 years of age, was diagnosed with hiv infection and was treated with APTIVUS. After drug was administered, patient experienced the following problems/side effects: haemarthrosis, haemorrhagic diathesis, injection site bruising, injection site haematoma, soft tissue haemorrhage, . APTIVUS dosage: TIPRANAVIR 1000 MG/RITONAVIR 400 MG. During the same period patient was treated with FUZEON. Patient recovered.

Mylotarg Side Effects Report #5592231-2
Physician from JAPAN reported MYLOTARG problem on Jan 11, 2008. Female patient, weighting 35.27 lb, was diagnosed with acute myeloid leukaemia recurrent, prophylaxis and was treated with MYLOTARG. After drug was administered, patient experienced the following problems/side effects: disseminated intravascular coagulation, haemorrhagic diathesis, oedema, . MYLOTARG dosage: unknown. During the same period patient was treated with ACYCLOVIR, BAKTAR, PRODIF, PANSPORIN. Patient was hospitalized. Patient recovered.

Kogenate Side Effects Report #5592753-4
KOGENATE problem was reported by a Health Professional from UNITED KINGDOM on Nov 30, 2007. Male patient, 40 years of age, was diagnosed with factor viii deficiency and was treated with KOGENATE. After drug was administered, patient experienced the following problems/side effects: factor viii inhibition, haemorrhagic diathesis, . KOGENATE dosage: unknown. Patient recovered.

Plavix Side Effects Report #5615917-X
Consumer or non-health professional from UNITED STATES reported PLAVIX problem on Nov 17, 2006. Male patient was diagnosed with cerebrovascular accident prophylaxis and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, haemorrhagic diathesis, . PLAVIX dosage: 75 MG QD - ORAL. During the same period patient was treated with ACETYLSALICYLIC ACID SRT. Patient recovered.

Plavix Side Effects Report #5621145-4
PLAVIX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 28, 2006. Male patient was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: eye haemorrhage, haemorrhagic diathesis, . PLAVIX dosage: unknown. Patient recovered.

Amoxicillin Side Effects Report #5547263-7
Consumer or non-health professional from SWITZERLAND reported AMOXICILLIN problem on Nov 30, 2007. Female patient, 58 years of age, was diagnosed with bacterial infection, pulmonary embolism and was treated with AMOXICILLIN. After drug was administered, patient experienced the following problems/side effects: haematoma, haemorrhagic diathesis, leukopenia, thrombocytopenia, . AMOXICILLIN dosage: unknown. During the same period patient was treated with DEXIBUPROFEN, MARCUMAR, MORPHINE ELIXIR, DURAGESIC, ELTROXIN, INDERAL, DIAMICRON, FLUANXOL. Patient recovered.

Kogenate Side Effects Report #5553598-4
KOGENATE problem was reported by a Health Professional from UNITED KINGDOM on Nov 30, 2007. Male patient, 40 years of age, was diagnosed with factor viii deficiency and was treated with KOGENATE. After drug was administered, patient experienced the following problems/side effects: factor viii inhibition, haemorrhagic diathesis, . KOGENATE dosage: unknown. Patient recovered.

Humira Side Effects Report #5558852-8
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Sept 10, 2007. Male patient, weighting 160.1 lb, was diagnosed with psoriatic arthropathy, glaucoma and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: dizziness, haemorrhagic diathesis, increased tendency to bruise, skin disorder, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOSOMAX, GLAUCOMA EYE DROPS. Patient recovered.

Humira Side Effects Report #5558992-3
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2007. Male patient, weighting 235.5 lb, was diagnosed with psoriasis, psoriatic arthropathy, diabetes mellitus, pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blister, haemorrhagic diathesis, increased tendency to bruise, skin atrophy, skin disorder, . HUMIRA dosage: unknown. During the same period patient was treated with METFORMIN, NAPROXEN. Patient recovered.

Humira Side Effects Report #5560402-7
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Nov 01, 2007. Male patient, weighting 116.1 lb, was diagnosed with crohn's disease, depression and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: burning sensation, haemorrhagic diathesis, increased tendency to bruise, libido decreased, rash, throat irritation, vomiting, . HUMIRA dosage: 160MG EVERY TWO WEEKS, THEN 80MG X1, AND THEN 40MG EVERY TWO WEEKS. During the same period patient was treated with AZATHIOPRINE, VENLAFAXIINE, BUPROPION. Patient recovered.