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

BLOOD GLUCOSE INCREASED ( 18 FDA reports)
WEIGHT DECREASED ( 18 FDA reports)
NAUSEA ( 17 FDA reports)
INJECTION SITE BRUISING ( 13 FDA reports)
DECREASED APPETITE ( 11 FDA reports)
INJECTION SITE HAEMORRHAGE ( 11 FDA reports)
INJECTION SITE PAIN ( 9 FDA reports)
DYSPEPSIA ( 7 FDA reports)
INJECTION SITE HAEMATOMA ( 7 FDA reports)
BLOOD GLUCOSE DECREASED ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
DIZZINESS ( 5 FDA reports)
INJECTION SITE EXTRAVASATION ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
COUGH ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HICCUPS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GOUT ( 2 FDA reports)
HUNGER ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INJECTION SITE LACERATION ( 2 FDA reports)
INJECTION SITE URTICARIA ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ARTHRITIS ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCAGON DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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