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RHEUMATOID FACTOR INCREASED side effect

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Myozyme Side Effects Report #5379544-4
Physician from UNITED STATES reported MYOZYME problem on June 19, 2007. Male patient, 22 years of age, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: condition aggravated, rheumatoid factor increased, serum sickness, synovial fluid white blood cells positive, . MYOZYME dosage: 20 MG/KG Q2WKS IV. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5379544-4
MYOZYME problem was reported by a Physician from UNITED STATES on June 19, 2007. Male patient, 22 years of age, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: condition aggravated, rheumatoid factor increased, serum sickness, synovial fluid white blood cells positive, . MYOZYME dosage: 20 MG/KG Q2WKS IV. Patient was hospitalized. Patient recovered.

Roaccutane Side Effects Report #5328714-X
Physician from SOUTH AFRICA reported ROACCUTANE problem on May 09, 2007. Female patient, 23 years of age, weighting 114.6 lb, was diagnosed with acne and was treated with ROACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthritis, rheumatoid factor increased, . ROACCUTANE dosage: REPORTED AS ROACCUTANED (INTERMITTENTLY). STRENGTH REPORTED AS 20 MG THEN 10 MG. FULL S WERE +. Patient recovered.

Depakene Side Effects Report #5283845-8
DEPAKENE problem was reported by a Health Professional from FRANCE on Mar 23, 2007. Male patient, 44 years of age, was treated with DEPAKENE. After drug was administered, patient experienced the following problems/side effects: neutropenia, rheumatoid factor increased, splenomegaly, white blood cell count increased, . DEPAKENE dosage: unknown. During the same period patient was treated with HEPARIN, RAMIPRIL, LORAZEPAM, NEXIUM, LOXEN PR. Patient was hospitalized. Patient recovered.


Loxen Side Effects Report #5290810-3
Consumer or non-health professional from JAPAN reported LOXEN LP problem on Mar 29, 2007. Male patient, 44 years of age, was treated with LOXEN LP. After drug was administered, patient experienced the following problems/side effects: neutropenia, rheumatoid factor increased, splenomegaly, . LOXEN LP dosage: unknown. During the same period patient was treated with DEPAKENE, TEMESTA, LOVENOX, NEXIUM, TRIATEC. Patient was hospitalized. Patient recovered.

Nicardipine Side Effects Report #5297418-4
NICARDIPINE HYDROCHLORIDE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 30, 2007. Male patient, 44 years of age, was treated with NICARDIPINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, rheumatoid factor increased, splenomegaly, white blood cell count increased, . NICARDIPINE HYDROCHLORIDE dosage: 50 MG; BID; PO. During the same period patient was treated with VALPROATE, LORAZEPAM, ENOXAPARIN, ESOMEPRAZOLE, RAMIPRIL. Patient was hospitalized. Patient recovered.

Roaccutane Side Effects Report #5306029-3
Physician from SOUTH AFRICA reported ROACCUTANE problem on Apr 13, 2007. Female patient, 24 years of age, was diagnosed with acne and was treated with ROACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthritis, rheumatoid factor increased, . ROACCUTANE dosage: REPORTED AS ROACCUTANED (INTERMITTENTLY). STRENGTH REPORTED AS 20 MG THEN 10 MG.. Patient recovered.

Nicardipine Side Effects Report #5306450-3
NICARDIPINE HYDROCHLORIDE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Apr 10, 2007. Male patient, 44 years of age, was treated with NICARDIPINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: neutropenia, rheumatoid factor increased, splenomegaly, . NICARDIPINE HYDROCHLORIDE dosage: 50 MG; BID; PO. During the same period patient was treated with VALPROATE, LORAZEPAM, ENOXAPARIN, ESOMEPRAZOLE MAGNESIUM, RAMIPRIL. Patient was hospitalized. Patient recovered.

Nicardipine Side Effects Report #5306502-8
Consumer or non-health professional from UNITED KINGDOM reported NICARDIPINE HYDROCHLORIDE problem on Apr 10, 2007. Male patient, 44 years of age, was treated with NICARDIPINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: neutropenia, rheumatoid factor increased, splenomegaly, white blood cell count increased, . NICARDIPINE HYDROCHLORIDE dosage: 50 MG; BID;PO. During the same period patient was treated with VALPROATE, LORAZEPAM, ENOXAPARIN, ESOMEPRAZOLE, RAMIPRIL. Patient was hospitalized. Patient recovered.


Nexium Side Effects Report #5312635-2
NEXIUM problem was reported by a Physician from UNITED STATES on Mar 08, 2007. Female patient, 72 years of age, weighting 158.1 lb, was diagnosed with gastrooesophageal reflux disease, erosive oesophagitis and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: bone pain, rheumatoid factor increased, . NEXIUM dosage: unknown. During the same period patient was treated with LIPITOR, VITAMIN CAP, FISH OIL. Patient recovered.

Depakene Side Effects Report #5269250-9
Health Professional from FRANCE reported DEPAKENE problem on Mar 09, 2007. Male patient, 44 years of age, was treated with DEPAKENE. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, rheumatoid factor increased, splenomegaly, white blood cell count increased, . DEPAKENE dosage: unknown. During the same period patient was treated with HEPARIN, RAMIPRIL, LORAZEPAM, NEXIUM, LOXEN PR. Patient was hospitalized. Patient recovered.

Lovenox Side Effects Report #5272340-8
LOVENOX problem was reported by a Consumer or non-health professional from on Mar 13, 2007. Male patient, 44 years of age, was treated with LOVENOX. After drug was administered, patient experienced the following problems/side effects: neutropenia, rheumatoid factor increased, splenomegaly, . LOVENOX dosage: unknown. During the same period patient was treated with TRIATEC, DEPAKENE, TEMESTA, NEXIUM, LOXEN. Patient was hospitalized. Patient recovered.

Loxen Side Effects Report #5281803-0
Consumer or non-health professional from JAPAN reported LOXEN LP problem on Mar 22, 2007. Male patient, 44 years of age, was treated with LOXEN LP. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, rheumatoid factor increased, splenomegaly, . LOXEN LP dosage: unknown. During the same period patient was treated with DEPAKENE, TEMESTA, LOVENOX, NEXIUM, TRIATEC. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5689531-4
CHANTIX problem was reported by a Health Professional from UNITED STATES on Mar 21, 2008. Male patient, 30 years of age, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: myalgia, pyrexia, rheumatoid factor increased, . CHANTIX dosage: unknown. Patient recovered.


Roaccutane Side Effects Report #5492192-0
Physician from SOUTH AFRICA reported ROACCUTANE problem on Oct 11, 2007. Female patient, 23 years of age, weighting 114.6 lb, was diagnosed with acne and was treated with ROACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthritis, hypothyroidism, rheumatoid factor increased, . ROACCUTANE dosage: REPORTED AS ROACCUTANE (INTERMITTENTLY). STRENGTH REPORTED AS 20 MG THEN 10 MG. FULL S WERE G+. Patient recovered.

Arava Side Effects Report #5700618-X
ARAVA problem was reported by a Consumer or non-health professional from AUSTRALIA on Apr 02, 2008. Female patient, 58 years of age, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, paralysis, rheumatoid factor increased, . ARAVA dosage: unknown. During the same period patient was treated with SALAZOPYRIN, PREDNISOLONE. Patient recovered.

Arava Side Effects Report #5717751-9
Consumer or non-health professional from AUSTRALIA reported ARAVA problem on Apr 21, 2008. Female patient, 58 years of age, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, paralysis, rheumatoid factor increased, . ARAVA dosage: unknown. During the same period patient was treated with SALAZOPYRIN, PREDNISOLONE. Patient recovered.

Roaccutane Side Effects Report #5337038-6
ROACCUTANE problem was reported by a Physician from SOUTH AFRICA on May 17, 2007. Female patient, 23 years of age, weighting 114.6 lb, was diagnosed with acne and was treated with ROACCUTANE. After drug was administered, patient experienced the following problems/side effects: arthritis, hypothyroidism, rheumatoid factor increased, . ROACCUTANE dosage: REPORTED AS ROACCUTANE (INTERMITTENTLY). STRENGTH REPORTED AS 20 MG THEN 10 MG. FULL S WERE G+. Patient recovered.