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

PRURITUS ( 8 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
CATARACT ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
COLITIS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)

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