Please choose an event type to view the corresponding MedsFacts report:

PYREXIA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMA ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
APOLIPOPROTEIN DECREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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