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

HYPOAESTHESIA ( 28 FDA reports)
ABDOMINAL PAIN LOWER ( 28 FDA reports)
VOMITING ( 28 FDA reports)
SPONDYLOARTHROPATHY ( 28 FDA reports)
ANKLE OPERATION ( 28 FDA reports)
ROAD TRAFFIC ACCIDENT ( 28 FDA reports)
AREFLEXIA ( 28 FDA reports)
PNEUMONIA ( 28 FDA reports)
ARTHROPATHY ( 28 FDA reports)
PELVIC PAIN ( 28 FDA reports)
OVARIAN CYST ( 28 FDA reports)
MUSCULAR WEAKNESS ( 28 FDA reports)
BREAST CYST ( 28 FDA reports)
BREAST PAIN ( 28 FDA reports)
BURSITIS ( 28 FDA reports)
MUSCLE ATROPHY ( 28 FDA reports)
MORTON'S NEUROMA ( 28 FDA reports)
MONONEUROPATHY ( 28 FDA reports)
MENOPAUSE ( 28 FDA reports)
MENISCUS LESION ( 28 FDA reports)
CYST ( 28 FDA reports)
DEAFNESS ( 28 FDA reports)
MECHANICAL URTICARIA ( 28 FDA reports)
DIARRHOEA ( 28 FDA reports)
DIZZINESS ( 28 FDA reports)
DYSPAREUNIA ( 28 FDA reports)
JOINT INSTABILITY ( 28 FDA reports)
FALL ( 28 FDA reports)
FATIGUE ( 28 FDA reports)
GENITAL RASH ( 28 FDA reports)
GAIT DISTURBANCE ( 28 FDA reports)
GASTRITIS ( 24 FDA reports)
FLANK PAIN ( 24 FDA reports)
HAEMORRHOIDS ( 24 FDA reports)
HEADACHE ( 24 FDA reports)
ABDOMINAL PAIN UPPER ( 24 FDA reports)
HYDRONEPHROSIS ( 24 FDA reports)
ABDOMINAL DISTENSION ( 24 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 24 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 24 FDA reports)
DYSPNOEA ( 24 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 24 FDA reports)
LIGAMENT DISORDER ( 24 FDA reports)
DECREASED APPETITE ( 24 FDA reports)
COUGH ( 24 FDA reports)
CONSTIPATION ( 24 FDA reports)
CHANGE OF BOWEL HABIT ( 24 FDA reports)
CALCULUS URETERIC ( 24 FDA reports)
BACK PAIN ( 24 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 24 FDA reports)
MYALGIA ( 24 FDA reports)
RADICULOPATHY ( 24 FDA reports)
NECK PAIN ( 24 FDA reports)
POLLAKIURIA ( 24 FDA reports)
AXILLARY PAIN ( 24 FDA reports)
PELVIC DEFORMITY ( 24 FDA reports)
AUTOIMMUNE INNER EAR DISEASE ( 24 FDA reports)
ARTHRALGIA ( 24 FDA reports)
CERVICOBRACHIAL SYNDROME ( 22 FDA reports)
PAIN IN EXTREMITY ( 22 FDA reports)
SKIN PAPILLOMA ( 20 FDA reports)
NAUSEA ( 18 FDA reports)
NIGHT SWEATS ( 18 FDA reports)
PYREXIA ( 18 FDA reports)
TENDONITIS ( 16 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
HOT FLUSH ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
RASH ( 8 FDA reports)
SLEEP DISORDER ( 8 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
APPENDICITIS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)

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